Canonical Allele Identifier: CA2678168459

Gene: HLA-DQA1

Linked Data

• gnomAD v4: 6-32642191-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642191_32642192insGG , CM000668.2:g.32642191_32642192insGG	GRCh38
NC_000006.11:g.32609968_32609969insGG , CM000668.1:g.32609968_32609969insGG	GRCh37
NC_000006.10:g.32717946_32717947insGG	NCBI36
NG_032876.1:g.9786_9787insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000343139.11:c.551_552insGG MANE Select	ENSP00000339398.5:p.Asp184GlufsTer19
ENST00000343139.9:c.551_552insGG	ENSP00000339398.5:p.Asp184GlufsTer19
ENST00000374949.2:c.551_552insGG	ENSP00000364087.2:p.Asp184GlufsTer19
ENST00000395363.5:c.551_552insGG	ENSP00000378767.1:p.Asp184GlufsTer19
ENST00000460633.1:n.579_580insGG
ENST00000482745.5:c.*1383_*1384insGG	ENSP00000436546.1:n.*1383_*1384insGG
ENST00000496318.5:c.551_552insGG	ENSP00000437302.1:p.Asp184GlufsTer19
NM_002122.3:c.551_552insGG	NP_002113.2:p.Asp184GlufsTer19
XM_006715079.2:c.551_552insGG	XP_006715142.1:p.Asp184GlufsTer19
XM_006715079.4:c.551_552insGG	XP_006715142.1:p.Asp184GlufsTer19
XR_001744085.1:n.86+396_86+397insCC
NM_002122.5:c.551_552insGG MANE Select	NP_002113.2:p.Asp184GlufsTer19