Canonical Allele Identifier: CA1618520094

Gene: HLA-A

Linked Data

• dbSNP Id: rs1771495126
• gnomAD v4: 6-29944880-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944881dup , CM000668.2:g.29944881dup	GRCh38
NC_000006.11:g.29912658dup , CM000668.1:g.29912658dup	GRCh37
NC_000006.10:g.30020637dup	NCBI36
NG_029217.2:g.7417dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.896-178dup	ENSP00000492789.2:n.896-178dup
ENST00000706892.1:n.2233dup
ENST00000706893.1:c.1065-178dup	ENSP00000516609.1:n.1065-178dup
ENST00000706894.1:c.1013-178dup	ENSP00000516610.1:n.1013-178dup
ENST00000706895.1:n.1655dup
ENST00000706896.1:n.2131dup
ENST00000706897.1:n.1553dup
ENST00000706898.1:c.1031-178dup	ENSP00000516611.1:n.1031-178dup
ENST00000706899.1:n.1867-178dup
ENST00000706900.1:c.929-178dup	ENSP00000516617.1:n.929-178dup
ENST00000706901.1:c.1013-178dup	ENSP00000516612.1:n.1013-178dup
ENST00000706902.1:c.1013-178dup	ENSP00000516613.1:n.1013-178dup
ENST00000706903.1:c.1013-178dup	ENSP00000516614.1:n.1013-178dup
ENST00000706904.1:c.1013-178dup	ENSP00000516615.1:n.1013-178dup
ENST00000706905.1:c.1013-178dup	ENSP00000516616.1:n.1013-178dup
ENST00000376809.10:c.1013-178dup MANE Select	ENSP00000366005.5:n.1013-178dup
ENST00000638375.1:c.896-178dup	ENSP00000492789.1:n.896-178dup
ENST00000376802.2:c.895+484dup	ENSP00000365998.2:n.895+484dup
ENST00000376806.9:c.1031-178dup	ENSP00000366002.5:n.1031-178dup
ENST00000376809.9:c.1013-178dup	ENSP00000366005.5:n.1013-178dup
ENST00000396634.5:c.1013-178dup	ENSP00000379873.1:n.1013-178dup
ENST00000461903.1:n.1272-178dup
ENST00000479320.5:n.1254-178dup
ENST00000495183.5:n.1256-182dup
ENST00000496081.5:n.1094dup
NM_002116.7:c.1013-178dup	NP_002107.3:n.1013-178dup
NM_002116.8:c.1013-178dup MANE Select	NP_002107.3:n.1013-178dup