Canonical Allele Identifier: CA363576816

Gene: HLA-DQA1

Linked Data

• gnomAD v4: 6-32642004-C-A
• MyVariant Identifiers: chr6:g.32609781C>A (hg19) ; chr6:g.32642004C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642004C>A , CM000668.2:g.32642004C>A	GRCh38
NC_000006.11:g.32609781C>A , CM000668.1:g.32609781C>A	GRCh37
NC_000006.10:g.32717759C>A	NCBI36
NG_032876.1:g.9599C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.364C>A MANE Select	ENSP00000339398.5:p.Pro122Thr
ENST00000343139.9:c.364C>A	ENSP00000339398.5:p.Pro122Thr
ENST00000374949.2:c.364C>A	ENSP00000364087.2:p.Pro122Thr
ENST00000395363.5:c.364C>A	ENSP00000378767.1:p.Pro122Thr
ENST00000460633.1:n.392C>A
ENST00000482745.5:c.*1196C>A	ENSP00000436546.1:n.*1196C>A
ENST00000496318.5:c.364C>A	ENSP00000437302.1:p.Pro122Thr
NM_002122.3:c.364C>A	NP_002113.2:p.Pro122Thr
XM_006715079.2:c.364C>A	XP_006715142.1:p.Pro122Thr
XM_006715079.4:c.364C>A	XP_006715142.1:p.Pro122Thr
XR_001744085.1:n.86+584G>T
NM_002122.5:c.364C>A MANE Select	NP_002113.2:p.Pro122Thr