Canonical Allele Identifier: CA1980654661

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406573C= , CM000673.2:g.68406573C=	GRCh38
NC_000011.9:g.68174041C= , CM000673.1:g.68174041C=	GRCh37
NC_000011.8:g.67930617C=	NCBI36
NG_015835.1:g.98934C=
NG_015835.2:g.98934C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1851C= MANE Select	ENSP00000294304.6:p.Phe617=
ENST00000294304.11:c.1851C=	ENSP00000294304.6:p.Phe617=
ENST00000529993.5:c.*457C=	ENSP00000436652.1:n.*457C=
NM_001291902.1:c.108C=	NP_001278831.1:p.Phe36=
NM_002335.3:c.1851C=	NP_002326.2:p.Phe617=
XM_005273994.2:c.1851C=	XP_005274051.1:p.Phe617=
XM_011545029.1:c.1878C=	XP_011543331.1:p.Phe626=
XM_011545030.1:c.1878C=	XP_011543332.1:p.Phe626=
XM_011545031.1:c.1878C=	XP_011543333.1:p.Phe626=
XR_949925.1:n.1893C=
XR_949926.1:n.1893C=
XM_017017735.1:c.108C=	XP_016873224.1:p.Phe36=
XR_001747874.1:n.1893C=
XR_949925.2:n.1893C=
XR_949926.2:n.1893C=
NM_002335.4:c.1851C= MANE Select	NP_002326.2:p.Phe617=
NM_001291902.2:c.108C=	NP_001278831.1:p.Phe36=