Canonical Allele Identifier: CA449461400

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944543-T-C
• MyVariant Identifiers: chr6:g.29912320T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944543T>C , CM000668.2:g.29944543T>C	GRCh38
NC_000006.11:g.29912320T>C , CM000668.1:g.29912320T>C	GRCh37
NC_000006.10:g.30020299T>C	NCBI36
NG_029217.2:g.7079T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+146T>C	ENSP00000492789.2:n.895+146T>C
ENST00000706892.1:n.1895T>C
ENST00000706893.1:c.973T>C	ENSP00000516609.1:p.Trp325Arg
ENST00000706894.1:c.939T>C	ENSP00000516610.1:p.Ala313=
ENST00000706895.1:n.1317T>C
ENST00000706896.1:n.1793T>C
ENST00000706897.1:n.1215T>C
ENST00000706898.1:c.939T>C	ENSP00000516611.1:p.Ala313=
ENST00000706899.1:n.1793T>C
ENST00000706900.1:c.855T>C	ENSP00000516617.1:p.Ala285=
ENST00000706901.1:c.939T>C	ENSP00000516612.1:p.Ala313=
ENST00000706902.1:c.939T>C	ENSP00000516613.1:p.Ala313=
ENST00000706903.1:c.939T>C	ENSP00000516614.1:p.Ala313=
ENST00000706904.1:c.939T>C	ENSP00000516615.1:p.Ala313=
ENST00000706905.1:c.939T>C	ENSP00000516616.1:p.Ala313=
ENST00000376809.10:c.939T>C MANE Select	ENSP00000366005.5:p.Ala313=
ENST00000638375.1:c.895+146T>C	ENSP00000492789.1:n.895+146T>C
ENST00000376802.2:c.895+146T>C	ENSP00000365998.2:n.895+146T>C
ENST00000376806.9:c.939T>C	ENSP00000366002.5:p.Ala313=
ENST00000376809.9:c.939T>C	ENSP00000366005.5:p.Ala313=
ENST00000396634.5:c.939T>C	ENSP00000379873.1:p.Ala313=
ENST00000461903.1:n.1180T>C
ENST00000479320.5:n.1180T>C
ENST00000495183.5:n.1182T>C
ENST00000496081.5:n.756T>C
NM_002116.7:c.939T>C	NP_002107.3:p.Ala313=
NM_002116.8:c.939T>C MANE Select	NP_002107.3:p.Ala313=