Transcript: ENST00000651502.1 CHRNG-203

Description

cholinergic receptor nicotinic gamma subunit [Source:HGNC Symbol;Acc:HGNC:1967]

Gene Synonyms

ACHRG

Location

Chromosome 2: 232,539,692-232,548,115 forward strand.

About this transcript

This transcript has 12 exons, is annotated with 28 domains and features, is associated with 4771 variant alleles and maps to 514 oligo probes.

Gene

This transcript is a product of gene ENSG00000196811.13 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000651502.1	CHRNG-203	4009	517aa	ENSP00000498757.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS33400	P07510-1	NM_005199.5	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENST00000389492.3	CHRNG-201	1398	465aa	ENSP00000374143.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		P07510-2	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENST00000485094.1	CHRNG-202	880	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,

Summary

Statistics

Exons: 12, Coding exons: 12, Transcript length: 4,009 bps, Translation length: 517 residues

MANE

This MANE Select transcript contains ENSP00000498757 and matches to NM_005199.5 and NP_005190.4

Uniprot

This transcript corresponds to the following Uniprot identifiers: P07510

CCDS

This transcript is a member of the Human CCDS set: CCDS33400

Version

ENST00000651502.1

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

Transcript: ENST00000651502.1 CHRNG-203

Summary

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Transcript: ENST00000651502.1 CHRNG-203

Summary

About Us

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