Canonical Allele Identifier: CA1980664406

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68446444C= , CM000673.2:g.68446444C=	GRCh38
NC_000011.9:g.68213912C= , CM000673.1:g.68213912C=	GRCh37
NC_000011.8:g.67970488C=	NCBI36
NG_015835.1:g.138805C=
NG_015835.2:g.138805C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4497C= MANE Select	ENSP00000294304.6:p.Asn1499=
ENST00000294304.11:c.4497C=	ENSP00000294304.6:p.Asn1499=
ENST00000529702.1:c.167C=
ENST00000529993.5:c.*3103C=	ENSP00000436652.1:n.*3103C=
NM_001291902.1:c.2754C=	NP_001278831.1:p.Asn918=
NM_002335.3:c.4497C=	NP_002326.2:p.Asn1499=
XM_005273994.2:c.4611C=	XP_005274051.1:p.Asn1537=
XM_011545029.1:c.4638C=	XP_011543331.1:p.Asn1546=
XM_011545030.1:c.4524C=	XP_011543332.1:p.Asn1508=
XM_011545031.1:c.4654C=	XP_011543333.1:p.Pro1552=
XR_949925.1:n.4653C=
XR_949926.1:n.4669C=
XM_017017735.1:c.2868C=	XP_016873224.1:p.Asn956=
XM_017017736.1:c.2151C=	XP_016873225.1:p.Asn717=
XR_949925.2:n.4653C=
XR_949926.2:n.4669C=
NM_002335.4:c.4497C= MANE Select	NP_002326.2:p.Asn1499=
NM_001291902.2:c.2754C=	NP_001278831.1:p.Asn918=