Canonical Allele Identifier: CA6149038

Gene: LRP5

Linked Data

• ClinVar Variation Id: 669010
• ClinVar RCV Id: RCV000827982
• dbSNP Id: rs80358306
• ExAC: 11:68125147 C / T
• gnomAD v2: 11-68125147-C-T
• gnomAD v3: 11-68357679-C-T
• gnomAD v4: 11-68357679-C-T
• MyVariant Identifiers: chr11:g.68125147C>T (hg19) ; chr11:g.68357679C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68357679C>T , CM000673.2:g.68357679C>T	GRCh38
NC_000011.9:g.68125147C>T , CM000673.1:g.68125147C>T	GRCh37
NC_000011.8:g.67881723C>T	NCBI36
NG_015835.1:g.50040C>T
NG_015835.2:g.50040C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.518C>T MANE Select	ENSP00000294304.6:p.Thr173Met
ENST00000294304.11:c.518C>T	ENSP00000294304.6:p.Thr173Met
ENST00000529993.5:c.518C>T	ENSP00000436652.1:p.Thr173Met
NM_001291902.1:c.-1248C>T	NP_001278831.1:n.-1248C>T
NM_002335.3:c.518C>T	NP_002326.2:p.Thr173Met
XM_005273994.2:c.518C>T	XP_005274051.1:p.Thr173Met
XM_011545029.1:c.545C>T	XP_011543331.1:p.Thr182Met
XM_011545030.1:c.545C>T	XP_011543332.1:p.Thr182Met
XM_011545031.1:c.545C>T	XP_011543333.1:p.Thr182Met
XR_949925.1:n.560C>T
XR_949926.1:n.560C>T
XR_001747874.1:n.560C>T
XR_949925.2:n.560C>T
XR_949926.2:n.560C>T
NM_002335.4:c.518C>T MANE Select	NP_002326.2:p.Thr173Met
NM_001291902.2:c.-1248C>T	NP_001278831.1:n.-1248C>T