Canonical Allele Identifier: CA1980654706

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406690C= , CM000673.2:g.68406690C=	GRCh38
NC_000011.9:g.68174158C= , CM000673.1:g.68174158C=	GRCh37
NC_000011.8:g.67930734C=	NCBI36
NG_015835.1:g.99051C=
NG_015835.2:g.99051C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1968C= MANE Select	ENSP00000294304.6:p.His656=
ENST00000294304.11:c.1968C=	ENSP00000294304.6:p.His656=
ENST00000529993.5:c.*574C=	ENSP00000436652.1:n.*574C=
NM_001291902.1:c.225C=	NP_001278831.1:p.His75=
NM_002335.3:c.1968C=	NP_002326.2:p.His656=
XM_005273994.2:c.1968C=	XP_005274051.1:p.His656=
XM_011545029.1:c.1995C=	XP_011543331.1:p.His665=
XM_011545030.1:c.1995C=	XP_011543332.1:p.His665=
XM_011545031.1:c.1995C=	XP_011543333.1:p.His665=
XR_949925.1:n.2010C=
XR_949926.1:n.2010C=
XM_017017735.1:c.225C=	XP_016873224.1:p.His75=
XR_001747874.1:n.2010C=
XR_949925.2:n.2010C=
XR_949926.2:n.2010C=
NM_002335.4:c.1968C= MANE Select	NP_002326.2:p.His656=
NM_001291902.2:c.225C=	NP_001278831.1:p.His75=