Canonical Allele Identifier: CA823967289

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs1251179292
• gnomAD v3: 6-32641666-AT-A
• gnomAD v4: 6-32641666-AT-A
• MyVariant Identifiers: chr6:g.32609444del (hg19) ; chr6:g.32641667del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641670del , CM000668.2:g.32641670del	GRCh38
NC_000006.11:g.32609447del , CM000668.1:g.32609447del	GRCh37
NC_000006.10:g.32717425del	NCBI36
NG_032876.1:g.9265del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.331+112del MANE Select	ENSP00000339398.5:n.331+112del
ENST00000343139.9:c.331+112del	ENSP00000339398.5:n.331+112del
ENST00000374949.2:c.331+112del	ENSP00000364087.2:n.331+112del
ENST00000395363.5:c.331+112del	ENSP00000378767.1:n.331+112del
ENST00000460633.1:n.359+112del
ENST00000482745.5:c.*1163+112del	ENSP00000436546.1:n.*1163+112del
ENST00000496318.5:c.331+112del	ENSP00000437302.1:n.331+112del
NM_002122.3:c.331+112del	NP_002113.2:n.331+112del
XM_006715079.2:c.331+112del	XP_006715142.1:n.331+112del
XM_006715079.4:c.331+112del	XP_006715142.1:n.331+112del
XR_001744085.1:n.86+921del
NM_002122.5:c.331+112del MANE Select	NP_002113.2:n.331+112del