Canonical Allele Identifier: CA449743731

Gene: HLA-DQA1

Linked Data

• gnomAD v4: 6-32641994-T-C
• MyVariant Identifiers: chr6:g.32609771T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641994T>C , CM000668.2:g.32641994T>C	GRCh38
NC_000006.11:g.32609771T>C , CM000668.1:g.32609771T>C	GRCh37
NC_000006.10:g.32717749T>C	NCBI36
NG_032876.1:g.9589T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000343139.11:c.354T>C MANE Select	ENSP00000339398.5:p.Phe118=
ENST00000343139.9:c.354T>C	ENSP00000339398.5:p.Phe118=
ENST00000374949.2:c.354T>C	ENSP00000364087.2:p.Phe118=
ENST00000395363.5:c.354T>C	ENSP00000378767.1:p.Phe118=
ENST00000460633.1:n.382T>C
ENST00000482745.5:c.*1186T>C	ENSP00000436546.1:n.*1186T>C
ENST00000496318.5:c.354T>C	ENSP00000437302.1:p.Phe118=
NM_002122.3:c.354T>C	NP_002113.2:p.Phe118=
XM_006715079.2:c.354T>C	XP_006715142.1:p.Phe118=
XM_006715079.4:c.354T>C	XP_006715142.1:p.Phe118=
XR_001744085.1:n.86+594A>G
NM_002122.5:c.354T>C MANE Select	NP_002113.2:p.Phe118=