Canonical Allele Identifier: CA1087604366

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs374819369
• gnomAD v3: 6-32641919-A-AGCTC
• gnomAD v4: 6-32641919-A-AGCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641919_32641920insGCTC , CM000668.2:g.32641919_32641920insGCTC	GRCh38
NC_000006.11:g.32609696_32609697insGCTC , CM000668.1:g.32609696_32609697insGCTC	GRCh37
NC_000006.10:g.32717674_32717675insGCTC	NCBI36
NG_032876.1:g.9514_9515insGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.332-53_332-52insGCTC MANE Select	ENSP00000339398.5:n.332-53_332-52insGCTC
ENST00000343139.9:c.332-53_332-52insGCTC	ENSP00000339398.5:n.332-53_332-52insGCTC
ENST00000374949.2:c.332-53_332-52insGCTC	ENSP00000364087.2:n.332-53_332-52insGCTC
ENST00000395363.5:c.332-53_332-52insGCTC	ENSP00000378767.1:n.332-53_332-52insGCTC
ENST00000460633.1:n.360-53_360-52insGCTC
ENST00000482745.5:c.*1164-53_*1164-52insGCTC	ENSP00000436546.1:n.*1164-53_*1164-52insGCTC
ENST00000496318.5:c.332-53_332-52insGCTC	ENSP00000437302.1:n.332-53_332-52insGCTC
NM_002122.3:c.332-53_332-52insGCTC	NP_002113.2:n.332-53_332-52insGCTC
XM_006715079.2:c.332-53_332-52insGCTC	XP_006715142.1:n.332-53_332-52insGCTC
XM_006715079.4:c.332-53_332-52insGCTC	XP_006715142.1:n.332-53_332-52insGCTC
XR_001744085.1:n.86+668_86+669insGAGC
NM_002122.5:c.332-53_332-52insGCTC MANE Select	NP_002113.2:n.332-53_332-52insGCTC