Canonical Allele Identifier: CA1980622101

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68433675C= , CM000673.2:g.68433675C=	GRCh38
NC_000011.9:g.68201143C= , CM000673.1:g.68201143C=	GRCh37
NC_000011.8:g.67957719C=	NCBI36
NG_015835.1:g.126036C=
NG_015835.2:g.126036C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.3837C= MANE Select	ENSP00000294304.6:p.Arg1279=
ENST00000294304.11:c.3837C=	ENSP00000294304.6:p.Arg1279=
ENST00000529993.5:c.*2443C=	ENSP00000436652.1:n.*2443C=
NM_001291902.1:c.2094C=	NP_001278831.1:p.Arg698=
NM_002335.3:c.3837C=	NP_002326.2:p.Arg1279=
XM_005273994.2:c.3837C=	XP_005274051.1:p.Arg1279=
XM_011545029.1:c.3864C=	XP_011543331.1:p.Arg1288=
XM_011545030.1:c.3864C=	XP_011543332.1:p.Arg1288=
XM_011545031.1:c.3864C=	XP_011543333.1:p.Arg1288=
XR_949925.1:n.3879C=
XR_949926.1:n.3879C=
XM_017017735.1:c.2094C=	XP_016873224.1:p.Arg698=
XM_017017736.1:c.1377C=	XP_016873225.1:p.Arg459=
XR_949925.2:n.3879C=
XR_949926.2:n.3879C=
NM_002335.4:c.3837C= MANE Select	NP_002326.2:p.Arg1279=
NM_001291902.2:c.2094C=	NP_001278831.1:p.Arg698=