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Human (GRCh38.p14)
Description

major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]

Location

Scaffold HSCHR6_MHC_MANN_CTG1: 1,195,801-1,200,442 forward strand.

GRCh38:GL000253.2

View this gene on the primary assembly.

About this gene

This gene has 9 transcripts (splice variants), 1 gene allele and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000456012.5HLA-A-2761868365aaENSP00000408986.1
 
Protein coding
B0UXQ0 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:NA
ENST00000550728.2HLA-A-2821611365aaENSP00000450169.1
 
Protein coding
B0UXQ0 -GENCODE BasicTSL:NA
ENST00000450342.5HLA-A-2751334299aaENSP00000391738.1
 
Protein coding
A0A140T941 -GENCODE BasicTSL:NA
ENST00000638576.1HLA-A-283975325aaENSP00000491864.1
 
Protein coding
A0A1W2PQS8 -GENCODE BasicTSL:NA
ENST00000470780.5HLA-A-2781856342aaENSP00000432736.1
 
Nonsense mediated decay
A0A140T9Z6 -TSL:NA
ENST00000492759.5HLA-A-2811784No protein-
 
Retained intron
--TSL:NA
ENST00000473059.5HLA-A-2791766No protein-
 
Retained intron
--TSL:NA
ENST00000462184.1HLA-A-2771354No protein-
 
Retained intron
--TSL:NA
ENST00000481018.5HLA-A-2801334No protein-
 
Retained intron
--TSL:NA