Canonical Allele Identifier: CA1111736031

Gene: HR

Linked Data

• gnomAD v3: 8-22116536-G-GCCCCCCCCC
• gnomAD v4: 8-22116536-G-GCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116537_22116538insCCCCCCCCC , CM000670.2:g.22116537_22116538insCCCCCCCCC	GRCh38
NC_000008.10:g.21974050_21974051insCCCCCCCCC , CM000670.1:g.21974050_21974051insCCCCCCCCC	GRCh37
NC_000008.9:g.22029995_22029996insCCCCCCCCC	NCBI36
NG_008166.1:g.18981_18982insGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3379-109_3379-108insGGGGGGGGG MANE Select	ENSP00000370826.4:n.3379-109_3379-108insGGGGGGGGG
ENST00000680789.1:c.3379-109_3379-108insGGGGGGGGG	ENSP00000505181.1:n.3379-109_3379-108insGGGGGGGGG
ENST00000312841.9:c.3214-109_3214-108insGGGGGGGGG	ENSP00000326765.8:n.3214-109_3214-108insGGGGGGGGG
ENST00000381418.8:c.3379-109_3379-108insGGGGGGGGG	ENSP00000370826.4:n.3379-109_3379-108insGGGGGGGGG
ENST00000522016.1:n.1572-109_1572-108insGGGGGGGGG
NM_005144.4:c.3379-109_3379-108insGGGGGGGGG	NP_005135.2:n.3379-109_3379-108insGGGGGGGGG
NM_018411.4:c.3214-109_3214-108insGGGGGGGGG	NP_060881.2:n.3214-109_3214-108insGGGGGGGGG
XM_005273569.1:c.3382-109_3382-108insGGGGGGGGG	XP_005273626.1:n.3382-109_3382-108insGGGGGGGGG
XM_006716367.1:c.3217-109_3217-108insGGGGGGGGG	XP_006716430.1:n.3217-109_3217-108insGGGGGGGGG
XM_005273569.2:c.3382-109_3382-108insGGGGGGGGG	XP_005273626.1:n.3382-109_3382-108insGGGGGGGGG
XM_006716367.2:c.3217-109_3217-108insGGGGGGGGG	XP_006716430.1:n.3217-109_3217-108insGGGGGGGGG
NM_005144.5:c.3379-109_3379-108insGGGGGGGGG MANE Select	NP_005135.2:n.3379-109_3379-108insGGGGGGGGG