Canonical Allele Identifier: CA1980666838

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68448822C= , CM000673.2:g.68448822C=	GRCh38
NC_000011.9:g.68216290C= , CM000673.1:g.68216290C=	GRCh37
NC_000011.8:g.67972866C=	NCBI36
NG_015835.1:g.141183C=
NG_015835.2:g.141183C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4600C= MANE Select	ENSP00000294304.6:p.Arg1534=
ENST00000294304.11:c.4600C=	ENSP00000294304.6:p.Arg1534=
ENST00000529481.1:n.191C=
ENST00000529702.1:c.270C=
ENST00000529993.5:c.*3206C=	ENSP00000436652.1:n.*3206C=
NM_001291902.1:c.2857C=	NP_001278831.1:p.Arg953=
NM_002335.3:c.4600C=	NP_002326.2:p.Arg1534=
XM_005273994.2:c.4714C=	XP_005274051.1:p.Arg1572=
XM_011545029.1:c.4741C=	XP_011543331.1:p.Arg1581=
XM_011545030.1:c.4627C=	XP_011543332.1:p.Arg1543=
XM_011545031.1:c.4757C=	XP_011543333.1:p.Ser1586=
XR_949925.1:n.4987C=
XR_949926.1:n.5003C=
XM_017017735.1:c.2971C=	XP_016873224.1:p.Arg991=
XM_017017736.1:c.2254C=	XP_016873225.1:p.Arg752=
XR_949925.2:n.4987C=
XR_949926.2:n.5003C=
NM_002335.4:c.4600C= MANE Select	NP_002326.2:p.Arg1534=
NM_001291902.2:c.2857C=	NP_001278831.1:p.Arg953=