Canonical Allele Identifier: CA363046351
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v3: 6-29944253-G-A
gnomAD v4: 6-29944253-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944253G>A , CM000668.2:g.29944253G>A GRCh38
NC_000006.11:g.29912030G>A , CM000668.1:g.29912030G>A GRCh37
NC_000006.10:g.30020009G>A NCBI36
NG_029217.2:g.6789G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.751G>A ENSP00000492789.2:p.Asp251Asn
ENST00000706892.1:n.1605G>A
ENST00000706893.1:c.751G>A ENSP00000516609.1:p.Asp251Asn
ENST00000706894.1:c.751G>A ENSP00000516610.1:p.Asp251Asn
ENST00000706895.1:n.1027G>A
ENST00000706896.1:n.1605G>A
ENST00000706897.1:n.1027G>A
ENST00000706898.1:c.751G>A ENSP00000516611.1:p.Asp251Asn
ENST00000706899.1:n.1605G>A
ENST00000706900.1:c.667G>A ENSP00000516617.1:p.Asp223Asn
ENST00000706901.1:c.751G>A ENSP00000516612.1:p.Asp251Asn
ENST00000706902.1:c.751G>A ENSP00000516613.1:p.Asp251Asn
ENST00000706903.1:c.751G>A ENSP00000516614.1:p.Asp251Asn
ENST00000706904.1:c.751G>A ENSP00000516615.1:p.Asp251Asn
ENST00000706905.1:c.751G>A ENSP00000516616.1:p.Asp251Asn
ENST00000376809.10:c.751G>A MANE Select ENSP00000366005.5:p.Asp251Asn
ENST00000638375.1:c.751G>A ENSP00000492789.1:p.Asp251Asn
ENST00000376802.2:c.751G>A ENSP00000365998.2:p.Asp251Asn
ENST00000376806.9:c.751G>A ENSP00000366002.5:p.Asp251Asn
ENST00000376809.9:c.751G>A ENSP00000366005.5:p.Asp251Asn
ENST00000396634.5:c.751G>A ENSP00000379873.1:p.Asp251Asn
ENST00000461903.1:n.992G>A
ENST00000479320.5:n.992G>A
ENST00000495183.5:n.994G>A
ENST00000496081.5:n.568G>A
NM_002116.7:c.751G>A NP_002107.3:p.Asp251Asn
NM_002116.8:c.751G>A MANE Select NP_002107.3:p.Asp251Asn