Human (GRCh38.p14)
Description

glutamate rich 1 [Source:HGNC Symbol;Acc:HGNC:27234]

Location
About this transcript

This transcript has 6 exons, is annotated with 16 domains and features, is associated with 45283 variant alleles and maps to 500 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000262109.8ERICH1-2011798443aaENSP00000262109.7
 
Protein coding
CCDS5955Q86X53 NM_207332.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000522893.1ERICH1-2073170223aaENSP00000428556.1
 
Protein coding
H0YB25 -TSL:1CDS 5' incomplete
ENST00000522706.5ERICH1-2061551345aaENSP00000428635.1
 
Protein coding
E5RHA3 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000523415.5ERICH1-2093630124aaENSP00000430296.1
 
Nonsense mediated decay
H0YBT6 -TSL:2CDS 5' incomplete
ENST00000518277.1ERICH1-202788No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000524138.5ERICH1-211682No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000519909.1ERICH1-205636No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000518895.1ERICH1-204585No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000523709.1ERICH1-210406No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000518313.1ERICH1-203287No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000523053.1ERICH1-208735No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 6, Coding exons: 6, Transcript length: 1,798 bps, Translation length: 443 residues

MANE

This MANE Select transcript contains ENSP00000262109 and matches to NM_207332.3 and NP_997215.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q86X53

CCDS

This transcript is a member of the Human CCDS set: CCDS5955

Transcript Support Level (TSL)

TSL:1

Version

ENST00000262109.8

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.