Description

T cell receptor alpha variable 21 [Source:HGNC Symbol;Acc:HGNC:12118]

Location
INSDC coordinates

chromosome:GRCh38:CM000676.2:22052514:22053056:1

About this gene

This gene has 1 transcript (splice variant), 28 orthologues, 22 paralogues and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtFlags
TRAV21-001ENST00000390449343112aaENSP00000452526
 
TR V geneGene that rearranges at the DNA level and codes the variable (V) region of the variable domain of T cell receptors.
-A0A0B4J279 CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:NA

Transcript Support Level Not Analysed. Pseudogenes, single exon transcripts, HLA, T-cell receptor and Ig transcripts are not analysed and therefore not given any of the TSL categories.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays