Canonical Allele Identifier: CA1980654694

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406646G= , CM000673.2:g.68406646G=	GRCh38
NC_000011.9:g.68174114G= , CM000673.1:g.68174114G=	GRCh37
NC_000011.8:g.67930690G=	NCBI36
NG_015835.1:g.99007G=
NG_015835.2:g.99007G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1924G= MANE Select	ENSP00000294304.6:p.Val642=
ENST00000294304.11:c.1924G=	ENSP00000294304.6:p.Val642=
ENST00000529993.5:c.*530G=	ENSP00000436652.1:n.*530G=
NM_001291902.1:c.181G=	NP_001278831.1:p.Val61=
NM_002335.3:c.1924G=	NP_002326.2:p.Val642=
XM_005273994.2:c.1924G=	XP_005274051.1:p.Val642=
XM_011545029.1:c.1951G=	XP_011543331.1:p.Val651=
XM_011545030.1:c.1951G=	XP_011543332.1:p.Val651=
XM_011545031.1:c.1951G=	XP_011543333.1:p.Val651=
XR_949925.1:n.1966G=
XR_949926.1:n.1966G=
XM_017017735.1:c.181G=	XP_016873224.1:p.Val61=
XR_001747874.1:n.1966G=
XR_949925.2:n.1966G=
XR_949926.2:n.1966G=
NM_002335.4:c.1924G= MANE Select	NP_002326.2:p.Val642=
NM_001291902.2:c.181G=	NP_001278831.1:p.Val61=