Canonical Allele Identifier: CA1087604369

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs1781454689
• gnomAD v3: 6-32641921-TTCAG-T
• gnomAD v4: 6-32641921-TTCAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641922_32641925del , CM000668.2:g.32641922_32641925del	GRCh38
NC_000006.11:g.32609699_32609702del , CM000668.1:g.32609699_32609702del	GRCh37
NC_000006.10:g.32717677_32717680del	NCBI36
NG_032876.1:g.9517_9520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.332-50_332-47del MANE Select	ENSP00000339398.5:n.332-50_332-47del
ENST00000343139.9:c.332-50_332-47del	ENSP00000339398.5:n.332-50_332-47del
ENST00000374949.2:c.332-50_332-47del	ENSP00000364087.2:n.332-50_332-47del
ENST00000395363.5:c.332-50_332-47del	ENSP00000378767.1:n.332-50_332-47del
ENST00000460633.1:n.360-50_360-47del
ENST00000482745.5:c.*1164-50_*1164-47del	ENSP00000436546.1:n.*1164-50_*1164-47del
ENST00000496318.5:c.332-50_332-47del	ENSP00000437302.1:n.332-50_332-47del
NM_002122.3:c.332-50_332-47del	NP_002113.2:n.332-50_332-47del
XM_006715079.2:c.332-50_332-47del	XP_006715142.1:n.332-50_332-47del
XM_006715079.4:c.332-50_332-47del	XP_006715142.1:n.332-50_332-47del
XR_001744085.1:n.86+663_86+666del
NM_002122.5:c.332-50_332-47del MANE Select	NP_002113.2:n.332-50_332-47del