Canonical Allele Identifier: CA381612147

Gene: LRP5

Linked Data

• ClinVar Variation Id: 1299476
• ClinVar RCV Id: RCV001728176
• dbSNP Id: rs2153153067
• gnomAD v4: 11-68386358-G-A
• MyVariant Identifiers: chr11:g.68153826G>A (hg19) ; chr11:g.68386358G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68386358G>A , CM000673.2:g.68386358G>A	GRCh38
NC_000011.9:g.68153826G>A , CM000673.1:g.68153826G>A	GRCh37
NC_000011.8:g.67910402G>A	NCBI36
NG_015835.1:g.78719G>A
NG_015835.2:g.78719G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.1058G>A MANE Select	ENSP00000294304.6:p.Arg353Gln
ENST00000294304.11:c.1058G>A	ENSP00000294304.6:p.Arg353Gln
ENST00000529993.5:c.1058G>A	ENSP00000436652.1:p.Arg353Gln
NM_001291902.1:c.-708G>A	NP_001278831.1:n.-708G>A
NM_002335.3:c.1058G>A	NP_002326.2:p.Arg353Gln
XM_005273994.2:c.1058G>A	XP_005274051.1:p.Arg353Gln
XM_011545029.1:c.1085G>A	XP_011543331.1:p.Arg362Gln
XM_011545030.1:c.1085G>A	XP_011543332.1:p.Arg362Gln
XM_011545031.1:c.1085G>A	XP_011543333.1:p.Arg362Gln
XR_949925.1:n.1100G>A
XR_949926.1:n.1100G>A
XR_001747874.1:n.1100G>A
XR_949925.2:n.1100G>A
XR_949926.2:n.1100G>A
NM_002335.4:c.1058G>A MANE Select	NP_002326.2:p.Arg353Gln
NM_001291902.2:c.-708G>A	NP_001278831.1:n.-708G>A