Human (GRCh38.p14)
Description

T cell leukemia translocation altered [Source:HGNC Symbol;Acc:HGNC:11692]

Location
About this transcript

This transcript has 3 exons, is annotated with 7 domains and features, is associated with 1787 variant alleles and maps to 319 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000273590.4TCTA-2011930103aaENSP00000273590.3
 
Protein coding
CCDS2796P57738 NM_022171.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000493381.1TCTA-2051081No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000487432.1TCTA-203892No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000488385.1TCTA-204800No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000482193.1TCTA-202590No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000497786.1TCTA-206587No protein-
 
Protein coding CDS not defined
--TSL:4
Statistics

Exons: 3, Coding exons: 3, Transcript length: 1,930 bps, Translation length: 103 residues

MANE

This MANE Select transcript contains ENSP00000273590 and matches to NM_022171.3 and NP_071503.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P57738

CCDS

This transcript is a member of the Human CCDS set: CCDS2796

Transcript Support Level (TSL)

TSL:1

Version

ENST00000273590.4

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.