Canonical Allele Identifier: CA363577085

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32642091-G-C
• gnomAD v4: 6-32642091-G-C
• MyVariant Identifiers: chr6:g.32609868G>C (hg19) ; chr6:g.32642091G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642091G>C , CM000668.2:g.32642091G>C	GRCh38
NC_000006.11:g.32609868G>C , CM000668.1:g.32609868G>C	GRCh37
NC_000006.10:g.32717846G>C	NCBI36
NG_032876.1:g.9686G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000343139.11:c.451G>C MANE Select	ENSP00000339398.5:p.Gly151Arg
ENST00000343139.9:c.451G>C	ENSP00000339398.5:p.Gly151Arg
ENST00000374949.2:c.451G>C	ENSP00000364087.2:p.Gly151Arg
ENST00000395363.5:c.451G>C	ENSP00000378767.1:p.Gly151Arg
ENST00000460633.1:n.479G>C
ENST00000482745.5:c.*1283G>C	ENSP00000436546.1:n.*1283G>C
ENST00000496318.5:c.451G>C	ENSP00000437302.1:p.Gly151Arg
NM_002122.3:c.451G>C	NP_002113.2:p.Gly151Arg
XM_006715079.2:c.451G>C	XP_006715142.1:p.Gly151Arg
XM_006715079.4:c.451G>C	XP_006715142.1:p.Gly151Arg
XR_001744085.1:n.86+497C>G
NM_002122.5:c.451G>C MANE Select	NP_002113.2:p.Gly151Arg