Canonical Allele Identifier: CA2573147533

Gene: LRP5

Linked Data

• ClinVar Variation Id: 1668754
• ClinVar RCV Id: RCV002194194
• dbSNP Id: rs2153167004

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68411416T>G , CM000673.2:g.68411416T>G	GRCh38
NC_000011.9:g.68178884T>G , CM000673.1:g.68178884T>G	GRCh37
NC_000011.8:g.67935460T>G	NCBI36
NG_015835.1:g.103777T>G
NG_015835.2:g.103777T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.2319-20T>G MANE Select	ENSP00000294304.6:n.2319-20T>G
ENST00000294304.11:c.2319-20T>G	ENSP00000294304.6:n.2319-20T>G
ENST00000528714.1:n.113-20T>G
ENST00000529993.5:c.*925-20T>G	ENSP00000436652.1:n.*925-20T>G
NM_001291902.1:c.576-20T>G	NP_001278831.1:n.576-20T>G
NM_002335.3:c.2319-20T>G	NP_002326.2:n.2319-20T>G
XM_005273994.2:c.2319-20T>G	XP_005274051.1:n.2319-20T>G
XM_011545029.1:c.2346-20T>G	XP_011543331.1:n.2346-20T>G
XM_011545030.1:c.2346-20T>G	XP_011543332.1:n.2346-20T>G
XM_011545031.1:c.2346-20T>G	XP_011543333.1:n.2346-20T>G
XR_949925.1:n.2361-20T>G
XR_949926.1:n.2361-20T>G
XM_017017735.1:c.576-20T>G	XP_016873224.1:n.576-20T>G
XR_001747874.1:n.2361-20T>G
XR_949925.2:n.2361-20T>G
XR_949926.2:n.2361-20T>G
NM_002335.4:c.2319-20T>G MANE Select	NP_002326.2:n.2319-20T>G
NM_001291902.2:c.576-20T>G	NP_001278831.1:n.576-20T>G