Canonical Allele Identifier: CA381617838

Gene: LRP5

Linked Data

• dbSNP Id: rs2098682837
• MyVariant Identifiers: chr11:g.68216293G>A (hg19) ; chr11:g.68448825G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68448825G>A , CM000673.2:g.68448825G>A	GRCh38
NC_000011.9:g.68216293G>A , CM000673.1:g.68216293G>A	GRCh37
NC_000011.8:g.67972869G>A	NCBI36
NG_015835.1:g.141186G>A
NG_015835.2:g.141186G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4603G>A MANE Select	ENSP00000294304.6:p.Gly1535Arg
ENST00000294304.11:c.4603G>A	ENSP00000294304.6:p.Gly1535Arg
ENST00000529481.1:n.194G>A
ENST00000529702.1:c.273G>A
ENST00000529993.5:c.*3209G>A	ENSP00000436652.1:n.*3209G>A
NM_001291902.1:c.2860G>A	NP_001278831.1:p.Gly954Arg
NM_002335.3:c.4603G>A	NP_002326.2:p.Gly1535Arg
XM_005273994.2:c.4717G>A	XP_005274051.1:p.Gly1573Arg
XM_011545029.1:c.4744G>A	XP_011543331.1:p.Gly1582Arg
XM_011545030.1:c.4630G>A	XP_011543332.1:p.Gly1544Arg
XM_011545031.1:c.4760G>A	XP_011543333.1:p.Arg1587Lys
XR_949925.1:n.4990G>A
XR_949926.1:n.5006G>A
XM_017017735.1:c.2974G>A	XP_016873224.1:p.Gly992Arg
XM_017017736.1:c.2257G>A	XP_016873225.1:p.Gly753Arg
XR_949925.2:n.4990G>A
XR_949926.2:n.5006G>A
NM_002335.4:c.4603G>A MANE Select	NP_002326.2:p.Gly1535Arg
NM_001291902.2:c.2860G>A	NP_001278831.1:p.Gly954Arg