Canonical Allele Identifier: CA1770254586

Gene: HR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116412C= , CM000670.2:g.22116412C=	GRCh38
NC_000008.10:g.21973925C= , CM000670.1:g.21973925C=	GRCh37
NC_000008.9:g.22029870C=	NCBI36
NG_008166.1:g.19106G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381418.9:c.3395G= MANE Select	ENSP00000370826.4:p.Ser1132=
ENST00000680789.1:c.3395G=	ENSP00000505181.1:p.Ser1132=
ENST00000312841.9:c.3230G=	ENSP00000326765.8:p.Ser1077=
ENST00000381418.8:c.3395G=	ENSP00000370826.4:p.Ser1132=
ENST00000522016.1:n.1588G=
NM_005144.4:c.3395G=	NP_005135.2:p.Ser1132=
NM_018411.4:c.3230G=	NP_060881.2:p.Ser1077=
XM_005273569.1:c.3398G=	XP_005273626.1:p.Ser1133=
XM_006716367.1:c.3233G=	XP_006716430.1:p.Ser1078=
XM_005273569.2:c.3398G=	XP_005273626.1:p.Ser1133=
XM_006716367.2:c.3233G=	XP_006716430.1:p.Ser1078=
NM_005144.5:c.3395G= MANE Select	NP_005135.2:p.Ser1132=