Canonical Allele Identifier: CA1980656706

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68448880G= , CM000673.2:g.68448880G=	GRCh38
NC_000011.9:g.68216348G= , CM000673.1:g.68216348G=	GRCh37
NC_000011.8:g.67972924G=	NCBI36
NG_015835.1:g.141241G=
NG_015835.2:g.141241G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.4658G= MANE Select	ENSP00000294304.6:p.Ser1553=
ENST00000294304.11:c.4658G=	ENSP00000294304.6:p.Ser1553=
ENST00000529481.1:n.249G=
ENST00000529702.1:c.328G=
ENST00000529993.5:c.*3264G=	ENSP00000436652.1:n.*3264G=
NM_001291902.1:c.2915G=	NP_001278831.1:p.Ser972=
NM_002335.3:c.4658G=	NP_002326.2:p.Ser1553=
XM_005273994.2:c.4772G=	XP_005274051.1:p.Ser1591=
XM_011545029.1:c.4799G=	XP_011543331.1:p.Ser1600=
XM_011545030.1:c.4685G=	XP_011543332.1:p.Ser1562=
XM_011545031.1:c.*12G=	XP_011543333.1:n.*12G=
XR_949925.1:n.5045G=
XR_949926.1:n.5061G=
XM_017017735.1:c.3029G=	XP_016873224.1:p.Ser1010=
XM_017017736.1:c.2312G=	XP_016873225.1:p.Ser771=
XR_949925.2:n.5045G=
XR_949926.2:n.5061G=
NM_002335.4:c.4658G= MANE Select	NP_002326.2:p.Ser1553=
NM_001291902.2:c.2915G=	NP_001278831.1:p.Ser972=