Canonical Allele Identifier: CA1087604146

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32641675-T-TTG
• gnomAD v4: 6-32641675-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641675_32641676insTG , CM000668.2:g.32641675_32641676insTG	GRCh38
NC_000006.11:g.32609452_32609453insTG , CM000668.1:g.32609452_32609453insTG	GRCh37
NC_000006.10:g.32717430_32717431insTG	NCBI36
NG_032876.1:g.9270_9271insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.331+117_331+118insTG MANE Select	ENSP00000339398.5:n.331+117_331+118insTG
ENST00000343139.9:c.331+117_331+118insTG	ENSP00000339398.5:n.331+117_331+118insTG
ENST00000374949.2:c.331+117_331+118insTG	ENSP00000364087.2:n.331+117_331+118insTG
ENST00000395363.5:c.331+117_331+118insTG	ENSP00000378767.1:n.331+117_331+118insTG
ENST00000460633.1:n.359+117_359+118insTG
ENST00000482745.5:c.*1163+117_*1163+118insTG	ENSP00000436546.1:n.*1163+117_*1163+118insTG
ENST00000496318.5:c.331+117_331+118insTG	ENSP00000437302.1:n.331+117_331+118insTG
NM_002122.3:c.331+117_331+118insTG	NP_002113.2:n.331+117_331+118insTG
XM_006715079.2:c.331+117_331+118insTG	XP_006715142.1:n.331+117_331+118insTG
XM_006715079.4:c.331+117_331+118insTG	XP_006715142.1:n.331+117_331+118insTG
XR_001744085.1:n.86+912_86+913insCA
NM_002122.5:c.331+117_331+118insTG MANE Select	NP_002113.2:n.331+117_331+118insTG