Canonical Allele Identifier: CA1980654643

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406538G= , CM000673.2:g.68406538G=	GRCh38
NC_000011.9:g.68174006G= , CM000673.1:g.68174006G=	GRCh37
NC_000011.8:g.67930582G=	NCBI36
NG_015835.1:g.98899G=
NG_015835.2:g.98899G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1816G= MANE Select	ENSP00000294304.6:p.Ala606=
ENST00000294304.11:c.1816G=	ENSP00000294304.6:p.Ala606=
ENST00000528890.1:n.455G=
ENST00000529993.5:c.*422G=	ENSP00000436652.1:n.*422G=
NM_001291902.1:c.73G=	NP_001278831.1:p.Ala25=
NM_002335.3:c.1816G=	NP_002326.2:p.Ala606=
XM_005273994.2:c.1816G=	XP_005274051.1:p.Ala606=
XM_011545029.1:c.1843G=	XP_011543331.1:p.Ala615=
XM_011545030.1:c.1843G=	XP_011543332.1:p.Ala615=
XM_011545031.1:c.1843G=	XP_011543333.1:p.Ala615=
XR_949925.1:n.1858G=
XR_949926.1:n.1858G=
XM_017017735.1:c.73G=	XP_016873224.1:p.Ala25=
XR_001747874.1:n.1858G=
XR_949925.2:n.1858G=
XR_949926.2:n.1858G=
NM_002335.4:c.1816G= MANE Select	NP_002326.2:p.Ala606=
NM_001291902.2:c.73G=	NP_001278831.1:p.Ala25=