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Human (GRCh38.p14)
Description

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

Location

Scaffold HSCHR6_MHC_SSTO_CTG1: 1,239,073-1,307,767 forward strand.

GRCh38:GL000256.2

View this gene on the primary assembly.

About this gene

This gene has 10 transcripts (splice variants), 1 gene allele and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000454091.5HLA-A-2371868365aaENSP00000410645.1
 
Protein coding
Q5RJ27 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:NA
ENST00000552493.4HLA-A-2431611365aaENSP00000448992.1
 
Protein coding
Q5RJ27 -GENCODE BasicTSL:NA
ENST00000638335.1HLA-A-2451600339aaENSP00000492821.1
 
Protein coding
A0A1W2PS39 -GENCODE BasicTSL:NA
ENST00000612644.2HLA-A-2441494326aaENSP00000480039.1
 
Protein coding
Q9GJ45 -GENCODE BasicTSL:NA
ENST00000414592.5HLA-A-2361334299aaENSP00000394582.1
 
Protein coding
A0A140T975 -GENCODE BasicTSL:NA
ENST00000488889.5HLA-A-2421856No protein-
 
Protein coding CDS not defined
--TSL:NA
ENST00000463148.5HLA-A-2391784No protein-
 
Retained intron
--TSL:NA
ENST00000464713.5HLA-A-2401766No protein-
 
Retained intron
--TSL:NA
ENST00000462986.1HLA-A-2381354No protein-
 
Retained intron
--TSL:NA
ENST00000478258.5HLA-A-2411334No protein-
 
Retained intron
--TSL:NA