Canonical Allele Identifier: CA137008369

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs796299429

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641736_32641737delinsTT , CM000668.2:g.32641736_32641737delinsTT	GRCh38
NC_000006.11:g.32609513_32609514delinsTT , CM000668.1:g.32609513_32609514delinsTT	GRCh37
NC_000006.10:g.32717491_32717492delinsTT	NCBI36
NG_032876.1:g.9331_9332delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.331+178_331+179delinsTT MANE Select	ENSP00000339398.5:n.331+178_331+179delinsTT
ENST00000343139.9:c.331+178_331+179delinsTT	ENSP00000339398.5:n.331+178_331+179delinsTT
ENST00000374949.2:c.331+178_331+179delinsTT	ENSP00000364087.2:n.331+178_331+179delinsTT
ENST00000395363.5:c.331+178_331+179delinsTT	ENSP00000378767.1:n.331+178_331+179delinsTT
ENST00000460633.1:n.359+178_359+179delinsTT
ENST00000482745.5:c.*1163+178_*1163+179delinsTT	ENSP00000436546.1:n.*1163+178_*1163+179delinsTT
ENST00000496318.5:c.331+178_331+179delinsTT	ENSP00000437302.1:n.331+178_331+179delinsTT
NM_002122.3:c.331+178_331+179delinsTT	NP_002113.2:n.331+178_331+179delinsTT
XM_006715079.2:c.331+178_331+179delinsTT	XP_006715142.1:n.331+178_331+179delinsTT
XM_006715079.4:c.331+178_331+179delinsTT	XP_006715142.1:n.331+178_331+179delinsTT
XR_001744085.1:n.86+851_86+852delinsAA
NM_002122.5:c.331+178_331+179delinsTT MANE Select	NP_002113.2:n.331+178_331+179delinsTT