Canonical Allele Identifier: CA2594790523

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32641873-G-GGA
• gnomAD v4: 6-32641873-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641874_32641875insAG , CM000668.2:g.32641874_32641875insAG	GRCh38
NC_000006.11:g.32609651_32609652insAG , CM000668.1:g.32609651_32609652insAG	GRCh37
NC_000006.10:g.32717629_32717630insAG	NCBI36
NG_032876.1:g.9469_9470insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.332-98_332-97insAG MANE Select	ENSP00000339398.5:n.332-98_332-97insAG
ENST00000343139.9:c.332-98_332-97insAG	ENSP00000339398.5:n.332-98_332-97insAG
ENST00000374949.2:c.332-98_332-97insAG	ENSP00000364087.2:n.332-98_332-97insAG
ENST00000395363.5:c.332-98_332-97insAG	ENSP00000378767.1:n.332-98_332-97insAG
ENST00000460633.1:n.360-98_360-97insAG
ENST00000482745.5:c.*1164-98_*1164-97insAG	ENSP00000436546.1:n.*1164-98_*1164-97insAG
ENST00000496318.5:c.332-98_332-97insAG	ENSP00000437302.1:n.332-98_332-97insAG
NM_002122.3:c.332-98_332-97insAG	NP_002113.2:n.332-98_332-97insAG
XM_006715079.2:c.332-98_332-97insAG	XP_006715142.1:n.332-98_332-97insAG
XM_006715079.4:c.332-98_332-97insAG	XP_006715142.1:n.332-98_332-97insAG
XR_001744085.1:n.86+714_86+715insTC
NM_002122.5:c.332-98_332-97insAG MANE Select	NP_002113.2:n.332-98_332-97insAG