Canonical Allele Identifier: CA1980666872

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68448834C= , CM000673.2:g.68448834C=	GRCh38
NC_000011.9:g.68216302C= , CM000673.1:g.68216302C=	GRCh37
NC_000011.8:g.67972878C=	NCBI36
NG_015835.1:g.141195C=
NG_015835.2:g.141195C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4612C= MANE Select	ENSP00000294304.6:p.Pro1538=
ENST00000294304.11:c.4612C=	ENSP00000294304.6:p.Pro1538=
ENST00000529481.1:n.203C=
ENST00000529702.1:c.282C=
ENST00000529993.5:c.*3218C=	ENSP00000436652.1:n.*3218C=
NM_001291902.1:c.2869C=	NP_001278831.1:p.Pro957=
NM_002335.3:c.4612C=	NP_002326.2:p.Pro1538=
XM_005273994.2:c.4726C=	XP_005274051.1:p.Pro1576=
XM_011545029.1:c.4753C=	XP_011543331.1:p.Pro1585=
XM_011545030.1:c.4639C=	XP_011543332.1:p.Pro1547=
XM_011545031.1:c.4769C=	XP_011543333.1:p.Ala1590=
XR_949925.1:n.4999C=
XR_949926.1:n.5015C=
XM_017017735.1:c.2983C=	XP_016873224.1:p.Pro995=
XM_017017736.1:c.2266C=	XP_016873225.1:p.Pro756=
XR_949925.2:n.4999C=
XR_949926.2:n.5015C=
NM_002335.4:c.4612C= MANE Select	NP_002326.2:p.Pro1538=
NM_001291902.2:c.2869C=	NP_001278831.1:p.Pro957=