Canonical Allele Identifier: CA136023370
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs199474521
gnomAD v4: 6-29943375-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943375A>T , CM000668.2:g.29943375A>T GRCh38
NC_000006.11:g.29911152A>T , CM000668.1:g.29911152A>T GRCh37
NC_000006.10:g.30019131A>T NCBI36
NG_029217.2:g.5910A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.451A>T ENSP00000492789.2:p.Asn151Tyr
ENST00000706892.1:n.727A>T
ENST00000706893.1:c.451A>T ENSP00000516609.1:p.Asn151Tyr
ENST00000706894.1:c.451A>T ENSP00000516610.1:p.Asn151Tyr
ENST00000706895.1:n.727A>T
ENST00000706896.1:n.727A>T
ENST00000706897.1:n.727A>T
ENST00000706898.1:c.451A>T ENSP00000516611.1:p.Asn151Tyr
ENST00000706899.1:n.727A>T
ENST00000706900.1:c.367A>T ENSP00000516617.1:p.Asn123Tyr
ENST00000706901.1:c.451A>T ENSP00000516612.1:p.Asn151Tyr
ENST00000706902.1:c.451A>T ENSP00000516613.1:p.Asn151Tyr
ENST00000706903.1:c.451A>T ENSP00000516614.1:p.Asn151Tyr
ENST00000706904.1:c.451A>T ENSP00000516615.1:p.Asn151Tyr
ENST00000706905.1:c.451A>T ENSP00000516616.1:p.Asn151Tyr
ENST00000376809.10:c.451A>T MANE Select ENSP00000366005.5:p.Asn151Tyr
ENST00000638375.1:c.451A>T ENSP00000492789.1:p.Asn151Tyr
ENST00000376802.2:c.451A>T ENSP00000365998.2:p.Asn151Tyr
ENST00000376806.9:c.451A>T ENSP00000366002.5:p.Asn151Tyr
ENST00000376809.9:c.451A>T ENSP00000366005.5:p.Asn151Tyr
ENST00000396634.5:c.451A>T ENSP00000379873.1:p.Asn151Tyr
ENST00000461903.1:n.692A>T
ENST00000479320.5:n.692A>T
ENST00000495183.5:n.694A>T
ENST00000496081.5:n.268A>T
NM_002116.7:c.451A>T NP_002107.3:p.Asn151Tyr
NM_002116.8:c.451A>T MANE Select NP_002107.3:p.Asn151Tyr