Canonical Allele Identifier: CA1770267984

Gene: HR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22123717C= , CM000670.2:g.22123717C=	GRCh38
NC_000008.10:g.21981230C= , CM000670.1:g.21981230C=	GRCh37
NC_000008.9:g.22037175C=	NCBI36
NG_008166.1:g.11801G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.1847G= MANE Select	ENSP00000370826.4:p.Arg616=
ENST00000680789.1:c.1847G=	ENSP00000505181.1:p.Arg616=
ENST00000312841.9:c.1847G=	ENSP00000326765.8:p.Arg616=
ENST00000381418.8:c.1847G=	ENSP00000370826.4:p.Arg616=
NM_005144.4:c.1847G=	NP_005135.2:p.Arg616=
NM_018411.4:c.1847G=	NP_060881.2:p.Arg616=
XM_005273569.1:c.1850G=	XP_005273626.1:p.Arg617=
XM_006716367.1:c.1850G=	XP_006716430.1:p.Arg617=
XM_005273569.2:c.1850G=	XP_005273626.1:p.Arg617=
XM_006716367.2:c.1850G=	XP_006716430.1:p.Arg617=
NM_005144.5:c.1847G= MANE Select	NP_005135.2:p.Arg616=