Canonical Allele Identifier: CA449379952

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945250-G-A
• MyVariant Identifiers: chr6:g.29913027G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945250G>A , CM000668.2:g.29945250G>A	GRCh38
NC_000006.11:g.29913027G>A , CM000668.1:g.29913027G>A	GRCh37
NC_000006.10:g.30021006G>A	NCBI36
NG_029217.2:g.7786G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.945G>A	ENSP00000492789.2:p.Gln315=
ENST00000706892.1:n.2602G>A
ENST00000706893.1:c.*46G>A	ENSP00000516609.1:n.*46G>A
ENST00000706894.1:c.1062G>A	ENSP00000516610.1:p.Gln354=
ENST00000706895.1:n.1882G>A
ENST00000706896.1:n.2358G>A
ENST00000706897.1:n.1780G>A
ENST00000706898.1:c.1080G>A	ENSP00000516611.1:p.Gln360=
ENST00000706899.1:n.1916G>A
ENST00000706900.1:c.978G>A	ENSP00000516617.1:p.Gln326=
ENST00000706901.1:c.1062G>A	ENSP00000516612.1:p.Gln354=
ENST00000706902.1:c.1062G>A	ENSP00000516613.1:p.Gln354=
ENST00000706903.1:c.1062G>A	ENSP00000516614.1:p.Gln354=
ENST00000706904.1:c.1062G>A	ENSP00000516615.1:p.Gln354=
ENST00000706905.1:c.1062G>A	ENSP00000516616.1:p.Gln354=
ENST00000376809.10:c.1062G>A MANE Select	ENSP00000366005.5:p.Gln354=
ENST00000638375.1:c.945G>A	ENSP00000492789.1:p.Gln315=
ENST00000376802.2:c.896-201G>A	ENSP00000365998.2:n.896-201G>A
ENST00000376806.9:c.1080G>A	ENSP00000366002.5:p.Gln360=
ENST00000376809.9:c.1062G>A	ENSP00000366005.5:p.Gln354=
ENST00000396634.5:c.1062G>A	ENSP00000379873.1:p.Gln354=
ENST00000461903.1:n.1321G>A
ENST00000479320.5:n.1303G>A
ENST00000495183.5:n.1301G>A
ENST00000496081.5:n.1321G>A
NM_002116.7:c.1062G>A	NP_002107.3:p.Gln354=
NM_002116.8:c.1062G>A MANE Select	NP_002107.3:p.Gln354=