Canonical Allele Identifier: CA449461488

Gene: HLA-A

Linked Data

• gnomAD v3: 6-29944318-G-T
• gnomAD v4: 6-29944318-G-T
• MyVariant Identifiers: chr6:g.29912095G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944318G>T , CM000668.2:g.29944318G>T	GRCh38
NC_000006.11:g.29912095G>T , CM000668.1:g.29912095G>T	GRCh37
NC_000006.10:g.30020074G>T	NCBI36
NG_029217.2:g.6854G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.816G>T	ENSP00000492789.2:p.Val272=
ENST00000706892.1:n.1670G>T
ENST00000706893.1:c.816G>T	ENSP00000516609.1:p.Val272=
ENST00000706894.1:c.816G>T	ENSP00000516610.1:p.Val272=
ENST00000706895.1:n.1092G>T
ENST00000706896.1:n.1670G>T
ENST00000706897.1:n.1092G>T
ENST00000706898.1:c.816G>T	ENSP00000516611.1:p.Val272=
ENST00000706899.1:n.1670G>T
ENST00000706900.1:c.732G>T	ENSP00000516617.1:p.Val244=
ENST00000706901.1:c.816G>T	ENSP00000516612.1:p.Val272=
ENST00000706902.1:c.816G>T	ENSP00000516613.1:p.Val272=
ENST00000706903.1:c.816G>T	ENSP00000516614.1:p.Val272=
ENST00000706904.1:c.816G>T	ENSP00000516615.1:p.Val272=
ENST00000706905.1:c.816G>T	ENSP00000516616.1:p.Val272=
ENST00000376809.10:c.816G>T MANE Select	ENSP00000366005.5:p.Val272=
ENST00000638375.1:c.816G>T	ENSP00000492789.1:p.Val272=
ENST00000376802.2:c.816G>T	ENSP00000365998.2:p.Val272=
ENST00000376806.9:c.816G>T	ENSP00000366002.5:p.Val272=
ENST00000376809.9:c.816G>T	ENSP00000366005.5:p.Val272=
ENST00000396634.5:c.816G>T	ENSP00000379873.1:p.Val272=
ENST00000461903.1:n.1057G>T
ENST00000479320.5:n.1057G>T
ENST00000495183.5:n.1059G>T
ENST00000496081.5:n.633G>T
NM_002116.7:c.816G>T	NP_002107.3:p.Val272=
NM_002116.8:c.816G>T MANE Select	NP_002107.3:p.Val272=