Canonical Allele Identifier: CA6149454

Gene: LRP5

Linked Data

• dbSNP Id: rs777696950
• ExAC: 11:68173951 G / A
• gnomAD v2: 11-68173951-G-A
• gnomAD v4: 11-68406483-G-A
• MyVariant Identifiers: chr11:g.68173951G>A (hg19) ; chr11:g.68406483G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406483G>A , CM000673.2:g.68406483G>A	GRCh38
NC_000011.9:g.68173951G>A , CM000673.1:g.68173951G>A	GRCh37
NC_000011.8:g.67930527G>A	NCBI36
NG_015835.1:g.98844G>A
NG_015835.2:g.98844G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1802-41G>A MANE Select	ENSP00000294304.6:n.1802-41G>A
ENST00000294304.11:c.1802-41G>A	ENSP00000294304.6:n.1802-41G>A
ENST00000528890.1:n.441-41G>A
ENST00000529993.5:c.*408-41G>A	ENSP00000436652.1:n.*408-41G>A
NM_001291902.1:c.59-41G>A	NP_001278831.1:n.59-41G>A
NM_002335.3:c.1802-41G>A	NP_002326.2:n.1802-41G>A
XM_005273994.2:c.1802-41G>A	XP_005274051.1:n.1802-41G>A
XM_011545029.1:c.1829-41G>A	XP_011543331.1:n.1829-41G>A
XM_011545030.1:c.1829-41G>A	XP_011543332.1:n.1829-41G>A
XM_011545031.1:c.1829-41G>A	XP_011543333.1:n.1829-41G>A
XR_949925.1:n.1844-41G>A
XR_949926.1:n.1844-41G>A
XM_017017735.1:c.59-41G>A	XP_016873224.1:n.59-41G>A
XR_001747874.1:n.1844-41G>A
XR_949925.2:n.1844-41G>A
XR_949926.2:n.1844-41G>A
NM_002335.4:c.1802-41G>A MANE Select	NP_002326.2:n.1802-41G>A
NM_001291902.2:c.59-41G>A	NP_001278831.1:n.59-41G>A