Canonical Allele Identifier: CA363577089

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32642094-C-A
• gnomAD v4: 6-32642094-C-A
• MyVariant Identifiers: chr6:g.32609871C>A (hg19) ; chr6:g.32642094C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642094C>A , CM000668.2:g.32642094C>A	GRCh38
NC_000006.11:g.32609871C>A , CM000668.1:g.32609871C>A	GRCh37
NC_000006.10:g.32717849C>A	NCBI36
NG_032876.1:g.9689C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.454C>A MANE Select	ENSP00000339398.5:p.Gln152Lys
ENST00000343139.9:c.454C>A	ENSP00000339398.5:p.Gln152Lys
ENST00000374949.2:c.454C>A	ENSP00000364087.2:p.Gln152Lys
ENST00000395363.5:c.454C>A	ENSP00000378767.1:p.Gln152Lys
ENST00000460633.1:n.482C>A
ENST00000482745.5:c.*1286C>A	ENSP00000436546.1:n.*1286C>A
ENST00000496318.5:c.454C>A	ENSP00000437302.1:p.Gln152Lys
NM_002122.3:c.454C>A	NP_002113.2:p.Gln152Lys
XM_006715079.2:c.454C>A	XP_006715142.1:p.Gln152Lys
XM_006715079.4:c.454C>A	XP_006715142.1:p.Gln152Lys
XR_001744085.1:n.86+494G>T
NM_002122.5:c.454C>A MANE Select	NP_002113.2:p.Gln152Lys