Canonical Allele Identifier: CA3693703
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs2231119
gnomAD v2: 6-29912856-A-T
gnomAD v3: 6-29945079-A-T
gnomAD v4: 6-29945079-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945079A>T , CM000668.2:g.29945079A>T GRCh38
NC_000006.11:g.29912856A>T , CM000668.1:g.29912856A>T GRCh37
NC_000006.10:g.30020835A>T NCBI36
NG_029217.2:g.7615A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.916A>T ENSP00000492789.2:p.Thr306Ser
ENST00000706892.1:n.2431A>T
ENST00000706893.1:c.*17A>T ENSP00000516609.1:n.*17A>T
ENST00000706894.1:c.1033A>T ENSP00000516610.1:p.Thr345Ser
ENST00000706895.1:n.1853A>T
ENST00000706896.1:n.2329A>T
ENST00000706897.1:n.1751A>T
ENST00000706898.1:c.1051A>T ENSP00000516611.1:p.Thr351Ser
ENST00000706899.1:n.1887A>T
ENST00000706900.1:c.949A>T ENSP00000516617.1:p.Thr317Ser
ENST00000706901.1:c.1033A>T ENSP00000516612.1:p.Thr345Ser
ENST00000706902.1:c.1033A>T ENSP00000516613.1:p.Thr345Ser
ENST00000706903.1:c.1033A>T ENSP00000516614.1:p.Thr345Ser
ENST00000706904.1:c.1033A>T ENSP00000516615.1:p.Thr345Ser
ENST00000706905.1:c.1033A>T ENSP00000516616.1:p.Thr345Ser
ENST00000376809.10:c.1033A>T MANE Select ENSP00000366005.5:p.Thr345Ser
ENST00000638375.1:c.916A>T ENSP00000492789.1:p.Thr306Ser
ENST00000376802.2:c.896-372A>T ENSP00000365998.2:n.896-372A>T
ENST00000376806.9:c.1051A>T ENSP00000366002.5:p.Thr351Ser
ENST00000376809.9:c.1033A>T ENSP00000366005.5:p.Thr345Ser
ENST00000396634.5:c.1033A>T ENSP00000379873.1:p.Thr345Ser
ENST00000461903.1:n.1292A>T
ENST00000479320.5:n.1274A>T
ENST00000495183.5:n.1272A>T
ENST00000496081.5:n.1292A>T
NM_002116.7:c.1033A>T NP_002107.3:p.Thr345Ser
NM_002116.8:c.1033A>T MANE Select NP_002107.3:p.Thr345Ser