Canonical Allele Identifier: CA1980639592

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68357579C= , CM000673.2:g.68357579C=	GRCh38
NC_000011.9:g.68125047C= , CM000673.1:g.68125047C=	GRCh37
NC_000011.8:g.67881623C=	NCBI36
NG_015835.1:g.49940C=
NG_015835.2:g.49940C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.489-71C= MANE Select	ENSP00000294304.6:n.489-71C=
ENST00000294304.11:c.489-71C=	ENSP00000294304.6:n.489-71C=
ENST00000529993.5:c.489-71C=	ENSP00000436652.1:n.489-71C=
NM_001291902.1:c.-1277-71C=	NP_001278831.1:n.-1277-71C=
NM_002335.3:c.489-71C=	NP_002326.2:n.489-71C=
XM_005273994.2:c.489-71C=	XP_005274051.1:n.489-71C=
XM_011545029.1:c.516-71C=	XP_011543331.1:n.516-71C=
XM_011545030.1:c.516-71C=	XP_011543332.1:n.516-71C=
XM_011545031.1:c.516-71C=	XP_011543333.1:n.516-71C=
XR_949925.1:n.531-71C=
XR_949926.1:n.531-71C=
XR_001747874.1:n.531-71C=
XR_949925.2:n.531-71C=
XR_949926.2:n.531-71C=
NM_002335.4:c.489-71C= MANE Select	NP_002326.2:n.489-71C=
NM_001291902.2:c.-1277-71C=	NP_001278831.1:n.-1277-71C=