Canonical Allele Identifier: CA1111736012

Gene: HR

Linked Data

• gnomAD v3: 8-22116529-A-ACCC
• gnomAD v4: 8-22116529-A-ACCC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116531_22116533dup , CM000670.2:g.22116531_22116533dup	GRCh38
NC_000008.10:g.21974044_21974046dup , CM000670.1:g.21974044_21974046dup	GRCh37
NC_000008.9:g.22029989_22029991dup	NCBI36
NG_008166.1:g.18986_18988dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3379-104_3379-102dup MANE Select	ENSP00000370826.4:n.3379-104_3379-102dup
ENST00000680789.1:c.3379-104_3379-102dup	ENSP00000505181.1:n.3379-104_3379-102dup
ENST00000312841.9:c.3214-104_3214-102dup	ENSP00000326765.8:n.3214-104_3214-102dup
ENST00000381418.8:c.3379-104_3379-102dup	ENSP00000370826.4:n.3379-104_3379-102dup
ENST00000522016.1:n.1572-104_1572-102dup
NM_005144.4:c.3379-104_3379-102dup	NP_005135.2:n.3379-104_3379-102dup
NM_018411.4:c.3214-104_3214-102dup	NP_060881.2:n.3214-104_3214-102dup
XM_005273569.1:c.3382-104_3382-102dup	XP_005273626.1:n.3382-104_3382-102dup
XM_006716367.1:c.3217-104_3217-102dup	XP_006716430.1:n.3217-104_3217-102dup
XM_005273569.2:c.3382-104_3382-102dup	XP_005273626.1:n.3382-104_3382-102dup
XM_006716367.2:c.3217-104_3217-102dup	XP_006716430.1:n.3217-104_3217-102dup
NM_005144.5:c.3379-104_3379-102dup MANE Select	NP_005135.2:n.3379-104_3379-102dup