Canonical Allele Identifier: CA1980645969

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68363884T= , CM000673.2:g.68363884T=	GRCh38
NC_000011.9:g.68131352T= , CM000673.1:g.68131352T=	GRCh37
NC_000011.8:g.67887928T=	NCBI36
NG_015835.1:g.56245T=
NG_015835.2:g.56245T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.824T= MANE Select	ENSP00000294304.6:p.Leu275=
ENST00000294304.11:c.824T=	ENSP00000294304.6:p.Leu275=
ENST00000529993.5:c.824T=	ENSP00000436652.1:p.Leu275=
NM_001291902.1:c.-942T=	NP_001278831.1:n.-942T=
NM_002335.3:c.824T=	NP_002326.2:p.Leu275=
XM_005273994.2:c.824T=	XP_005274051.1:p.Leu275=
XM_011545029.1:c.851T=	XP_011543331.1:p.Leu284=
XM_011545030.1:c.851T=	XP_011543332.1:p.Leu284=
XM_011545031.1:c.851T=	XP_011543333.1:p.Leu284=
XR_949925.1:n.866T=
XR_949926.1:n.866T=
XR_001747874.1:n.866T=
XR_949925.2:n.866T=
XR_949926.2:n.866T=
NM_002335.4:c.824T= MANE Select	NP_002326.2:p.Leu275=
NM_001291902.2:c.-942T=	NP_001278831.1:n.-942T=