Canonical Allele Identifier: CA917717086

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs1561946503

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641675_32641676delinsCT , CM000668.2:g.32641675_32641676delinsCT	GRCh38
NC_000006.11:g.32609452_32609453delinsCT , CM000668.1:g.32609452_32609453delinsCT	GRCh37
NC_000006.10:g.32717430_32717431delinsCT	NCBI36
NG_032876.1:g.9270_9271delinsCT

Transcript Alleles

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