Canonical Allele Identifier: CA2678168108

Gene: HLA-DQA1

Linked Data

• gnomAD v4: 6-32641676-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641676_32641677insCT , CM000668.2:g.32641676_32641677insCT	GRCh38
NC_000006.11:g.32609453_32609454insCT , CM000668.1:g.32609453_32609454insCT	GRCh37
NC_000006.10:g.32717431_32717432insCT	NCBI36
NG_032876.1:g.9271_9272insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.331+118_331+119insCT MANE Select	ENSP00000339398.5:n.331+118_331+119insCT
ENST00000343139.9:c.331+118_331+119insCT	ENSP00000339398.5:n.331+118_331+119insCT
ENST00000374949.2:c.331+118_331+119insCT	ENSP00000364087.2:n.331+118_331+119insCT
ENST00000395363.5:c.331+118_331+119insCT	ENSP00000378767.1:n.331+118_331+119insCT
ENST00000460633.1:n.359+118_359+119insCT
ENST00000482745.5:c.*1163+118_*1163+119insCT	ENSP00000436546.1:n.*1163+118_*1163+119insCT
ENST00000496318.5:c.331+118_331+119insCT	ENSP00000437302.1:n.331+118_331+119insCT
NM_002122.3:c.331+118_331+119insCT	NP_002113.2:n.331+118_331+119insCT
XM_006715079.2:c.331+118_331+119insCT	XP_006715142.1:n.331+118_331+119insCT
XM_006715079.4:c.331+118_331+119insCT	XP_006715142.1:n.331+118_331+119insCT
XR_001744085.1:n.86+911_86+912insAG
NM_002122.5:c.331+118_331+119insCT MANE Select	NP_002113.2:n.331+118_331+119insCT