Canonical Allele Identifier: CA1087604329

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs2150967942
• gnomAD v3: 6-32641876-G-GA
• gnomAD v4: 6-32641876-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641876_32641877insA , CM000668.2:g.32641876_32641877insA	GRCh38
NC_000006.11:g.32609653_32609654insA , CM000668.1:g.32609653_32609654insA	GRCh37
NC_000006.10:g.32717631_32717632insA	NCBI36
NG_032876.1:g.9471_9472insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.332-96_332-95insA MANE Select	ENSP00000339398.5:n.332-96_332-95insA
ENST00000343139.9:c.332-96_332-95insA	ENSP00000339398.5:n.332-96_332-95insA
ENST00000374949.2:c.332-96_332-95insA	ENSP00000364087.2:n.332-96_332-95insA
ENST00000395363.5:c.332-96_332-95insA	ENSP00000378767.1:n.332-96_332-95insA
ENST00000460633.1:n.360-96_360-95insA
ENST00000482745.5:c.*1164-96_*1164-95insA	ENSP00000436546.1:n.*1164-96_*1164-95insA
ENST00000496318.5:c.332-96_332-95insA	ENSP00000437302.1:n.332-96_332-95insA
NM_002122.3:c.332-96_332-95insA	NP_002113.2:n.332-96_332-95insA
XM_006715079.2:c.332-96_332-95insA	XP_006715142.1:n.332-96_332-95insA
XM_006715079.4:c.332-96_332-95insA	XP_006715142.1:n.332-96_332-95insA
XR_001744085.1:n.86+711_86+712insT
NM_002122.5:c.332-96_332-95insA MANE Select	NP_002113.2:n.332-96_332-95insA