Canonical Allele Identifier: CA363048593
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v4: 6-29945238-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945238T>A , CM000668.2:g.29945238T>A GRCh38
NC_000006.11:g.29913015T>A , CM000668.1:g.29913015T>A GRCh37
NC_000006.10:g.30020994T>A NCBI36
NG_029217.2:g.7774T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.933T>A ENSP00000492789.2:p.Ser311Arg
ENST00000706892.1:n.2590T>A
ENST00000706893.1:c.*34T>A ENSP00000516609.1:n.*34T>A
ENST00000706894.1:c.1050T>A ENSP00000516610.1:p.Ser350Arg
ENST00000706895.1:n.1870T>A
ENST00000706896.1:n.2346T>A
ENST00000706897.1:n.1768T>A
ENST00000706898.1:c.1068T>A ENSP00000516611.1:p.Ser356Arg
ENST00000706899.1:n.1904T>A
ENST00000706900.1:c.966T>A ENSP00000516617.1:p.Ser322Arg
ENST00000706901.1:c.1050T>A ENSP00000516612.1:p.Ser350Arg
ENST00000706902.1:c.1050T>A ENSP00000516613.1:p.Ser350Arg
ENST00000706903.1:c.1050T>A ENSP00000516614.1:p.Ser350Arg
ENST00000706904.1:c.1050T>A ENSP00000516615.1:p.Ser350Arg
ENST00000706905.1:c.1050T>A ENSP00000516616.1:p.Ser350Arg
ENST00000376809.10:c.1050T>A MANE Select ENSP00000366005.5:p.Ser350Arg
ENST00000638375.1:c.933T>A ENSP00000492789.1:p.Ser311Arg
ENST00000376802.2:c.896-213T>A ENSP00000365998.2:n.896-213T>A
ENST00000376806.9:c.1068T>A ENSP00000366002.5:p.Ser356Arg
ENST00000376809.9:c.1050T>A ENSP00000366005.5:p.Ser350Arg
ENST00000396634.5:c.1050T>A ENSP00000379873.1:p.Ser350Arg
ENST00000461903.1:n.1309T>A
ENST00000479320.5:n.1291T>A
ENST00000495183.5:n.1289T>A
ENST00000496081.5:n.1309T>A
NM_002116.7:c.1050T>A NP_002107.3:p.Ser350Arg
NM_002116.8:c.1050T>A MANE Select NP_002107.3:p.Ser350Arg