Canonical Allele Identifier: CA1111735961

Gene: HR

Linked Data

• gnomAD v3: 8-22116518-A-ACCCCCC
• gnomAD v4: 8-22116518-A-ACCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116518_22116519insCCCCCC , CM000670.2:g.22116518_22116519insCCCCCC	GRCh38
NC_000008.10:g.21974031_21974032insCCCCCC , CM000670.1:g.21974031_21974032insCCCCCC	GRCh37
NC_000008.9:g.22029976_22029977insCCCCCC	NCBI36
NG_008166.1:g.18999_19000insGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3379-91_3379-90insGGGGGG MANE Select	ENSP00000370826.4:n.3379-91_3379-90insGGGGGG
ENST00000680789.1:c.3379-91_3379-90insGGGGGG	ENSP00000505181.1:n.3379-91_3379-90insGGGGGG
ENST00000312841.9:c.3214-91_3214-90insGGGGGG	ENSP00000326765.8:n.3214-91_3214-90insGGGGGG
ENST00000381418.8:c.3379-91_3379-90insGGGGGG	ENSP00000370826.4:n.3379-91_3379-90insGGGGGG
ENST00000522016.1:n.1572-91_1572-90insGGGGGG
NM_005144.4:c.3379-91_3379-90insGGGGGG	NP_005135.2:n.3379-91_3379-90insGGGGGG
NM_018411.4:c.3214-91_3214-90insGGGGGG	NP_060881.2:n.3214-91_3214-90insGGGGGG
XM_005273569.1:c.3382-91_3382-90insGGGGGG	XP_005273626.1:n.3382-91_3382-90insGGGGGG
XM_006716367.1:c.3217-91_3217-90insGGGGGG	XP_006716430.1:n.3217-91_3217-90insGGGGGG
XM_005273569.2:c.3382-91_3382-90insGGGGGG	XP_005273626.1:n.3382-91_3382-90insGGGGGG
XM_006716367.2:c.3217-91_3217-90insGGGGGG	XP_006716430.1:n.3217-91_3217-90insGGGGGG
NM_005144.5:c.3379-91_3379-90insGGGGGG MANE Select	NP_005135.2:n.3379-91_3379-90insGGGGGG