Canonical Allele Identifier: CA1979429422

Gene: MUS81

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65862463G= , CM000673.2:g.65862463G=	GRCh38
NC_000011.9:g.65629934G= , CM000673.1:g.65629934G=	GRCh37
NC_000011.8:g.65386510G=	NCBI36
NG_053116.1:g.7402G=

Transcript Alleles

HGVS	Amino-acid Change
NM_025128.5:c.539G= MANE Select	NP_079404.3:p.Arg180=
ENST00000308110.9:c.539G= MANE Select	ENSP00000307853.4:p.Arg180=
NM_001350283.1:c.539G=	NP_001337212.1:p.Arg180=
NM_001350283.2:c.539G=	NP_001337212.1:p.Arg180=
NM_025128.4:c.539G=	NP_079404.3:p.Arg180=
NR_146598.1:n.892G=
NR_146598.2:n.860G=
ENST00000308110.8:c.539G=	ENSP00000307853.4:p.Arg180=
ENST00000524647.5:c.433G=
ENST00000525768.5:c.314G=	ENSP00000431478.1:p.Arg105=
ENST00000529374.5:c.312G=
ENST00000530111.1:c.225G=
ENST00000531905.1:n.777G=
ENST00000533035.5:c.314G=	ENSP00000432287.1:p.Arg105=
ENST00000533555.5:n.327G=
XM_005274307.1:c.539G=	XP_005274364.1:p.Arg180=
XM_011545269.1:c.539G=	XP_011543571.1:p.Arg180=
XM_011545270.1:c.539G=	XP_011543572.1:p.Arg180=
XM_011545271.1:c.539G=	XP_011543573.1:p.Arg180=
XR_001747984.1:n.707G=
XR_001747985.1:n.707G=
XR_001747986.1:n.707G=
XR_247212.2:n.707G=
XR_247212.3:n.707G=
XR_950067.1:n.707G=
XR_950067.2:n.707G=