Canonical Allele Identifier: CA1980654662

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406579A= , CM000673.2:g.68406579A=	GRCh38
NC_000011.9:g.68174047A= , CM000673.1:g.68174047A=	GRCh37
NC_000011.8:g.67930623A=	NCBI36
NG_015835.1:g.98940A=
NG_015835.2:g.98940A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1857A= MANE Select	ENSP00000294304.6:p.Thr619=
ENST00000294304.11:c.1857A=	ENSP00000294304.6:p.Thr619=
ENST00000529993.5:c.*463A=	ENSP00000436652.1:n.*463A=
NM_001291902.1:c.114A=	NP_001278831.1:p.Thr38=
NM_002335.3:c.1857A=	NP_002326.2:p.Thr619=
XM_005273994.2:c.1857A=	XP_005274051.1:p.Thr619=
XM_011545029.1:c.1884A=	XP_011543331.1:p.Thr628=
XM_011545030.1:c.1884A=	XP_011543332.1:p.Thr628=
XM_011545031.1:c.1884A=	XP_011543333.1:p.Thr628=
XR_949925.1:n.1899A=
XR_949926.1:n.1899A=
XM_017017735.1:c.114A=	XP_016873224.1:p.Thr38=
XR_001747874.1:n.1899A=
XR_949925.2:n.1899A=
XR_949926.2:n.1899A=
NM_002335.4:c.1857A= MANE Select	NP_002326.2:p.Thr619=
NM_001291902.2:c.114A=	NP_001278831.1:p.Thr38=