Human (GRCh38.p14)
Description

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

Location

Scaffold HSCHR6_MHC_DBB_CTG1: 1,144,955-1,265,390 forward strand.

GRCh38:GL000252.2

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
ENST00000438861.6HLA-A-2831854371aaENSP00000388526.2
 
Protein coding
A0A140T913 -Ensembl CanonicalGENCODE basicTSL:NA
ENST00000457879.5HLA-A-2851868365aaENSP00000403575.1
 
Protein coding
Q53Z42 -GENCODE basicTSL:NA
ENST00000547271.2HLA-A-2901611365aaENSP00000447962.1
 
Protein coding
Q53Z42 -GENCODE basicTSL:NA
ENST00000453975.5HLA-A-2841334299aaENSP00000392547.1
 
Protein coding
A0A140T955 -GENCODE basicTSL:NA
ENST00000638608.1HLA-A-2911307339aaENSP00000491527.1
 
Protein coding
A0A1W2PPQ2 -GENCODE basicTSL:NA
ENST00000640080.1HLA-A-2921094362aaENSP00000492489.1
 
Protein coding
A0A1W2PRT9 -GENCODE basicTSL:NA
ENST00000468666.5HLA-A-2871782No protein-
 
Retained intron
--TSL:NA
ENST00000487534.5HLA-A-2891766No protein-
 
Retained intron
--TSL:NA
ENST00000470534.1HLA-A-2881352No protein-
 
Retained intron
--TSL:NA
ENST00000460542.5HLA-A-2861334No protein-
 
Retained intron
--TSL:NA