Canonical Allele Identifier: CA1980650275

Gene: LRP5

Linked Data

• dbSNP Id: rs491347

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68402220G>C , CM000673.2:g.68402220G>C	GRCh38
NC_000011.9:g.68169688G>C , CM000673.1:g.68169688G>C	GRCh37
NC_000011.8:g.67926264G>C	NCBI36
NG_015835.1:g.94581G>C
NG_015835.2:g.94581G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.1585-1263G>C MANE Select	ENSP00000294304.6:n.1585-1263G>C
ENST00000294304.11:c.1585-1263G>C	ENSP00000294304.6:n.1585-1263G>C
ENST00000529993.5:c.1413-1263G>C	ENSP00000436652.1:n.1413-1263G>C
NM_001291902.1:c.-353-1263G>C	NP_001278831.1:n.-353-1263G>C
NM_002335.3:c.1585-1263G>C	NP_002326.2:n.1585-1263G>C
XM_005273994.2:c.1585-1263G>C	XP_005274051.1:n.1585-1263G>C
XM_011545029.1:c.1612-1263G>C	XP_011543331.1:n.1612-1263G>C
XM_011545030.1:c.1612-1263G>C	XP_011543332.1:n.1612-1263G>C
XM_011545031.1:c.1612-1263G>C	XP_011543333.1:n.1612-1263G>C
XR_949925.1:n.1627-1263G>C
XR_949926.1:n.1627-1263G>C
XR_001747874.1:n.1627-1263G>C
XR_949925.2:n.1627-1263G>C
XR_949926.2:n.1627-1263G>C
NM_002335.4:c.1585-1263G>C MANE Select	NP_002326.2:n.1585-1263G>C
NM_001291902.2:c.-353-1263G>C	NP_001278831.1:n.-353-1263G>C