Canonical Allele Identifier: CA363047709
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v4: 6-29944506-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944506C>T , CM000668.2:g.29944506C>T GRCh38
NC_000006.11:g.29912283C>T , CM000668.1:g.29912283C>T GRCh37
NC_000006.10:g.30020262C>T NCBI36
NG_029217.2:g.7042C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.895+109C>T ENSP00000492789.2:n.895+109C>T
ENST00000706892.1:n.1858C>T
ENST00000706893.1:c.936C>T ENSP00000516609.1:p.Val312=
ENST00000706894.1:c.902C>T ENSP00000516610.1:p.Ser301Phe
ENST00000706895.1:n.1280C>T
ENST00000706896.1:n.1756C>T
ENST00000706897.1:n.1178C>T
ENST00000706898.1:c.902C>T ENSP00000516611.1:p.Ser301Phe
ENST00000706899.1:n.1756C>T
ENST00000706900.1:c.818C>T ENSP00000516617.1:p.Ser273Phe
ENST00000706901.1:c.902C>T ENSP00000516612.1:p.Ser301Phe
ENST00000706902.1:c.902C>T ENSP00000516613.1:p.Ser301Phe
ENST00000706903.1:c.902C>T ENSP00000516614.1:p.Ser301Phe
ENST00000706904.1:c.902C>T ENSP00000516615.1:p.Ser301Phe
ENST00000706905.1:c.902C>T ENSP00000516616.1:p.Ser301Phe
ENST00000376809.10:c.902C>T MANE Select ENSP00000366005.5:p.Ser301Phe
ENST00000638375.1:c.895+109C>T ENSP00000492789.1:n.895+109C>T
ENST00000376802.2:c.895+109C>T ENSP00000365998.2:n.895+109C>T
ENST00000376806.9:c.902C>T ENSP00000366002.5:p.Ser301Phe
ENST00000376809.9:c.902C>T ENSP00000366005.5:p.Ser301Phe
ENST00000396634.5:c.902C>T ENSP00000379873.1:p.Ser301Phe
ENST00000461903.1:n.1143C>T
ENST00000479320.5:n.1143C>T
ENST00000495183.5:n.1145C>T
ENST00000496081.5:n.719C>T
NM_002116.7:c.902C>T NP_002107.3:p.Ser301Phe
NM_002116.8:c.902C>T MANE Select NP_002107.3:p.Ser301Phe