Canonical Allele Identifier: CA1980638870

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68389861G= , CM000673.2:g.68389861G=	GRCh38
NC_000011.9:g.68157329G= , CM000673.1:g.68157329G=	GRCh37
NC_000011.8:g.67913905G=	NCBI36
NG_015835.1:g.82222G=
NG_015835.2:g.82222G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.1413-20G= MANE Select	ENSP00000294304.6:n.1413-20G=
ENST00000294304.11:c.1413-20G=	ENSP00000294304.6:n.1413-20G=
ENST00000529993.5:c.1412+3149G=	ENSP00000436652.1:n.1412+3149G=
NM_001291902.1:c.-354+3149G=	NP_001278831.1:n.-354+3149G=
NM_002335.3:c.1413-20G=	NP_002326.2:n.1413-20G=
XM_005273994.2:c.1413-20G=	XP_005274051.1:n.1413-20G=
XM_011545029.1:c.1440-20G=	XP_011543331.1:n.1440-20G=
XM_011545030.1:c.1440-20G=	XP_011543332.1:n.1440-20G=
XM_011545031.1:c.1440-20G=	XP_011543333.1:n.1440-20G=
XR_949925.1:n.1455-20G=
XR_949926.1:n.1455-20G=
XR_001747874.1:n.1455-20G=
XR_949925.2:n.1455-20G=
XR_949926.2:n.1455-20G=
NM_002335.4:c.1413-20G= MANE Select	NP_002326.2:n.1413-20G=
NM_001291902.2:c.-354+3149G=	NP_001278831.1:n.-354+3149G=