Canonical Allele Identifier: CA136024692
Gene: HLA-A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs199474621

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944225G>A , CM000668.2:g.29944225G>A GRCh38
NC_000006.11:g.29912002G>A , CM000668.1:g.29912002G>A GRCh37
NC_000006.10:g.30019981G>A NCBI36
NG_029217.2:g.6761G>A

Transcript Alleles

HGVS Amino-acid change
NM_002116.7:c.723G>A VV NP_002107.3:p.Trp241Ter
NM_002116.8:c.723G>A VV MANE Preferred NP_002107.3:p.Trp241Ter
ENST00000376802.2:c.723G>A ENSP00000365998.2:p.Trp241Ter
ENST00000376806.9:c.723G>A ENSP00000366002.5:p.Trp241Ter
ENST00000376809.9:c.723G>A ENSP00000366005.5:p.Trp241Ter
ENST00000396634.5:c.723G>A ENSP00000379873.1:p.Trp241Ter
ENST00000461903.1:n.964G>A
ENST00000479320.5:n.964G>A
ENST00000495183.5:n.966G>A
ENST00000496081.5:n.540G>A