Canonical Allele Identifier: CA1980617409

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68436969T= , CM000673.2:g.68436969T=	GRCh38
NC_000011.9:g.68204437T= , CM000673.1:g.68204437T=	GRCh37
NC_000011.8:g.67961013T=	NCBI36
NG_015835.1:g.129330T=
NG_015835.2:g.129330T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.4081T= MANE Select	ENSP00000294304.6:p.Cys1361=
ENST00000294304.11:c.4081T=	ENSP00000294304.6:p.Cys1361=
ENST00000529993.5:c.*2687T=	ENSP00000436652.1:n.*2687T=
NM_001291902.1:c.2338T=	NP_001278831.1:p.Cys780=
NM_002335.3:c.4081T=	NP_002326.2:p.Cys1361=
XM_005273994.2:c.4081T=	XP_005274051.1:p.Cys1361=
XM_011545029.1:c.4108T=	XP_011543331.1:p.Cys1370=
XM_011545030.1:c.4108T=	XP_011543332.1:p.Cys1370=
XM_011545031.1:c.4108T=	XP_011543333.1:p.Cys1370=
XR_949925.1:n.4123T=
XR_949926.1:n.4123T=
XM_017017735.1:c.2338T=	XP_016873224.1:p.Cys780=
XM_017017736.1:c.1621T=	XP_016873225.1:p.Cys541=
XR_949925.2:n.4123T=
XR_949926.2:n.4123T=
NM_002335.4:c.4081T= MANE Select	NP_002326.2:p.Cys1361=
NM_001291902.2:c.2338T=	NP_001278831.1:p.Cys780=