Canonical Allele Identifier: CA1980597940

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68413747C= , CM000673.2:g.68413747C=	GRCh38
NC_000011.9:g.68181215C= , CM000673.1:g.68181215C=	GRCh37
NC_000011.8:g.67937791C=	NCBI36
NG_015835.1:g.106108C=
NG_015835.2:g.106108C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.2562C= MANE Select	ENSP00000294304.6:p.Tyr854=
ENST00000294304.11:c.2562C=	ENSP00000294304.6:p.Tyr854=
ENST00000529993.5:c.*1168C=	ENSP00000436652.1:n.*1168C=
NM_001291902.1:c.819C=	NP_001278831.1:p.Tyr273=
NM_002335.3:c.2562C=	NP_002326.2:p.Tyr854=
XM_005273994.2:c.2562C=	XP_005274051.1:p.Tyr854=
XM_011545029.1:c.2589C=	XP_011543331.1:p.Tyr863=
XM_011545030.1:c.2589C=	XP_011543332.1:p.Tyr863=
XM_011545031.1:c.2589C=	XP_011543333.1:p.Tyr863=
XR_949925.1:n.2604C=
XR_949926.1:n.2604C=
XM_017017735.1:c.819C=	XP_016873224.1:p.Tyr273=
XM_017017736.1:c.102C=	XP_016873225.1:p.Tyr34=
XR_001747874.1:n.2828C=
XR_949925.2:n.2604C=
XR_949926.2:n.2604C=
NM_002335.4:c.2562C= MANE Select	NP_002326.2:p.Tyr854=
NM_001291902.2:c.819C=	NP_001278831.1:p.Tyr273=