Canonical Allele Identifier: CA1980666852

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68448825G= , CM000673.2:g.68448825G=	GRCh38
NC_000011.9:g.68216293G= , CM000673.1:g.68216293G=	GRCh37
NC_000011.8:g.67972869G=	NCBI36
NG_015835.1:g.141186G=
NG_015835.2:g.141186G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4603G= MANE Select	ENSP00000294304.6:p.Gly1535=
ENST00000294304.11:c.4603G=	ENSP00000294304.6:p.Gly1535=
ENST00000529481.1:n.194G=
ENST00000529702.1:c.273G=
ENST00000529993.5:c.*3209G=	ENSP00000436652.1:n.*3209G=
NM_001291902.1:c.2860G=	NP_001278831.1:p.Gly954=
NM_002335.3:c.4603G=	NP_002326.2:p.Gly1535=
XM_005273994.2:c.4717G=	XP_005274051.1:p.Gly1573=
XM_011545029.1:c.4744G=	XP_011543331.1:p.Gly1582=
XM_011545030.1:c.4630G=	XP_011543332.1:p.Gly1544=
XM_011545031.1:c.4760G=	XP_011543333.1:p.Arg1587=
XR_949925.1:n.4990G=
XR_949926.1:n.5006G=
XM_017017735.1:c.2974G=	XP_016873224.1:p.Gly992=
XM_017017736.1:c.2257G=	XP_016873225.1:p.Gly753=
XR_949925.2:n.4990G=
XR_949926.2:n.5006G=
NM_002335.4:c.4603G= MANE Select	NP_002326.2:p.Gly1535=
NM_001291902.2:c.2860G=	NP_001278831.1:p.Gly954=