Human (GRCh38.p14)
Description

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

Location

Scaffold HSCHR6_MHC_MCF_CTG1: 1,286,636-1,289,979 forward strand.

GRCh38:GL000254.2

View this gene on the primary assembly.

About this gene

This gene has 7 transcripts (splice variants), 1 gene allele and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000455882.5HLA-A-2581543371aaENSP00000416233.1
 
Protein coding
A0A140T9X5 -Ensembl CanonicalGENCODE basicTSL:NACDS 5' incomplete
ENST00000453057.5HLA-A-2571525365aaENSP00000403922.1
 
Protein coding
A0A140T9I0 -TSL:NACDS 5' incomplete
ENST00000413609.5HLA-A-2561327299aaENSP00000390225.1
 
Protein coding
A0A140T933 -TSL:NACDS 5' incomplete
ENST00000478186.1HLA-A-2611774No protein-
 
Retained intron
--TSL:NA
ENST00000471291.5HLA-A-2591762No protein-
 
Retained intron
--TSL:NA
ENST00000476132.5HLA-A-2601350No protein-
 
Retained intron
--TSL:NA
ENST00000479494.5HLA-A-2621332No protein-
 
Retained intron
--TSL:NA