Canonical Allele Identifier: CA1980654663

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406582C= , CM000673.2:g.68406582C=	GRCh38
NC_000011.9:g.68174050C= , CM000673.1:g.68174050C=	GRCh37
NC_000011.8:g.67930626C=	NCBI36
NG_015835.1:g.98943C=
NG_015835.2:g.98943C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.1860C= MANE Select	ENSP00000294304.6:p.Pro620=
ENST00000294304.11:c.1860C=	ENSP00000294304.6:p.Pro620=
ENST00000529993.5:c.*466C=	ENSP00000436652.1:n.*466C=
NM_001291902.1:c.117C=	NP_001278831.1:p.Pro39=
NM_002335.3:c.1860C=	NP_002326.2:p.Pro620=
XM_005273994.2:c.1860C=	XP_005274051.1:p.Pro620=
XM_011545029.1:c.1887C=	XP_011543331.1:p.Pro629=
XM_011545030.1:c.1887C=	XP_011543332.1:p.Pro629=
XM_011545031.1:c.1887C=	XP_011543333.1:p.Pro629=
XR_949925.1:n.1902C=
XR_949926.1:n.1902C=
XM_017017735.1:c.117C=	XP_016873224.1:p.Pro39=
XR_001747874.1:n.1902C=
XR_949925.2:n.1902C=
XR_949926.2:n.1902C=
NM_002335.4:c.1860C= MANE Select	NP_002326.2:p.Pro620=
NM_001291902.2:c.117C=	NP_001278831.1:p.Pro39=