Canonical Allele Identifier: CA449461434

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944567-G-T
• MyVariant Identifiers: chr6:g.29912344G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944567G>T , CM000668.2:g.29944567G>T	GRCh38
NC_000006.11:g.29912344G>T , CM000668.1:g.29912344G>T	GRCh37
NC_000006.10:g.30020323G>T	NCBI36
NG_029217.2:g.7103G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.895+170G>T	ENSP00000492789.2:n.895+170G>T
ENST00000706892.1:n.1919G>T
ENST00000706893.1:c.997G>T	ENSP00000516609.1:p.Asp333Tyr
ENST00000706894.1:c.963G>T	ENSP00000516610.1:p.Val321=
ENST00000706895.1:n.1341G>T
ENST00000706896.1:n.1817G>T
ENST00000706897.1:n.1239G>T
ENST00000706898.1:c.963G>T	ENSP00000516611.1:p.Val321=
ENST00000706899.1:n.1817G>T
ENST00000706900.1:c.879G>T	ENSP00000516617.1:p.Val293=
ENST00000706901.1:c.963G>T	ENSP00000516612.1:p.Val321=
ENST00000706902.1:c.963G>T	ENSP00000516613.1:p.Val321=
ENST00000706903.1:c.963G>T	ENSP00000516614.1:p.Val321=
ENST00000706904.1:c.963G>T	ENSP00000516615.1:p.Val321=
ENST00000706905.1:c.963G>T	ENSP00000516616.1:p.Val321=
ENST00000376809.10:c.963G>T MANE Select	ENSP00000366005.5:p.Val321=
ENST00000638375.1:c.895+170G>T	ENSP00000492789.1:n.895+170G>T
ENST00000376802.2:c.895+170G>T	ENSP00000365998.2:n.895+170G>T
ENST00000376806.9:c.963G>T	ENSP00000366002.5:p.Val321=
ENST00000376809.9:c.963G>T	ENSP00000366005.5:p.Val321=
ENST00000396634.5:c.963G>T	ENSP00000379873.1:p.Val321=
ENST00000461903.1:n.1204G>T
ENST00000479320.5:n.1204G>T
ENST00000495183.5:n.1206G>T
ENST00000496081.5:n.780G>T
NM_002116.7:c.963G>T	NP_002107.3:p.Val321=
NM_002116.8:c.963G>T MANE Select	NP_002107.3:p.Val321=