Canonical Allele Identifier: CA1980654700

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406678A= , CM000673.2:g.68406678A=	GRCh38
NC_000011.9:g.68174146A= , CM000673.1:g.68174146A=	GRCh37
NC_000011.8:g.67930722A=	NCBI36
NG_015835.1:g.99039A=
NG_015835.2:g.99039A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1956A= MANE Select	ENSP00000294304.6:p.Arg652=
ENST00000294304.11:c.1956A=	ENSP00000294304.6:p.Arg652=
ENST00000529993.5:c.*562A=	ENSP00000436652.1:n.*562A=
NM_001291902.1:c.213A=	NP_001278831.1:p.Arg71=
NM_002335.3:c.1956A=	NP_002326.2:p.Arg652=
XM_005273994.2:c.1956A=	XP_005274051.1:p.Arg652=
XM_011545029.1:c.1983A=	XP_011543331.1:p.Arg661=
XM_011545030.1:c.1983A=	XP_011543332.1:p.Arg661=
XM_011545031.1:c.1983A=	XP_011543333.1:p.Arg661=
XR_949925.1:n.1998A=
XR_949926.1:n.1998A=
XM_017017735.1:c.213A=	XP_016873224.1:p.Arg71=
XR_001747874.1:n.1998A=
XR_949925.2:n.1998A=
XR_949926.2:n.1998A=
NM_002335.4:c.1956A= MANE Select	NP_002326.2:p.Arg652=
NM_001291902.2:c.213A=	NP_001278831.1:p.Arg71=