Canonical Allele Identifier: CA15475770
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs112525507
gnomAD v2: 6-29913515-C-T
gnomAD v3: 6-29945738-C-T
gnomAD v4: 6-29945738-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945738C>T , CM000668.2:g.29945738C>T GRCh38
NC_000006.11:g.29913515C>T , CM000668.1:g.29913515C>T GRCh37
NC_000006.10:g.30021494C>T NCBI36
NG_029217.2:g.8274C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.1264C>T ENSP00000492789.2:n.1264C>T
ENST00000706894.1:c.*365C>T ENSP00000516610.1:n.*365C>T
ENST00000706895.1:n.2370C>T
ENST00000706896.1:n.2677C>T
ENST00000706897.1:n.2099C>T
ENST00000706898.1:c.*283C>T ENSP00000516611.1:n.*283C>T
ENST00000706899.1:n.2235C>T
ENST00000706900.1:c.*283C>T ENSP00000516617.1:n.*283C>T
ENST00000706901.1:c.*283C>T ENSP00000516612.1:n.*283C>T
ENST00000706902.1:c.1093+457C>T ENSP00000516613.1:n.1093+457C>T
ENST00000706903.1:c.*124+159C>T ENSP00000516614.1:n.*124+159C>T
ENST00000706904.1:c.1093+457C>T ENSP00000516615.1:n.1093+457C>T
ENST00000706905.1:c.*283C>T ENSP00000516616.1:n.*283C>T
ENST00000376809.10:c.*283C>T MANE Select ENSP00000366005.5:n.*283C>T
ENST00000376802.2:c.*283C>T ENSP00000365998.2:n.*283C>T
ENST00000376806.9:c.*283C>T ENSP00000366002.5:n.*283C>T
ENST00000376809.9:c.*283C>T ENSP00000366005.5:n.*283C>T
ENST00000396634.5:c.*283C>T ENSP00000379873.1:n.*283C>T
ENST00000495183.5:n.1620C>T
ENST00000496081.5:n.1640C>T
NM_002116.7:c.*283C>T NP_002107.3:n.*283C>T
NM_002116.8:c.*283C>T MANE Select NP_002107.3:n.*283C>T