Canonical Allele Identifier: CA6149485

Gene: LRP5

Linked Data

• ClinVar Variation Id: 1989899
• ClinVar RCV Id: RCV002786741
• dbSNP Id: rs368392203
• ExAC: 11:68174104 G / T
• gnomAD v2: 11-68174104-G-T
• gnomAD v3: 11-68406636-G-T
• gnomAD v4: 11-68406636-G-T
• MyVariant Identifiers: chr11:g.68174104G>T (hg19) ; chr11:g.68406636G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406636G>T , CM000673.2:g.68406636G>T	GRCh38
NC_000011.9:g.68174104G>T , CM000673.1:g.68174104G>T	GRCh37
NC_000011.8:g.67930680G>T	NCBI36
NG_015835.1:g.98997G>T
NG_015835.2:g.98997G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1914G>T MANE Select	ENSP00000294304.6:p.Lys638Asn
ENST00000294304.11:c.1914G>T	ENSP00000294304.6:p.Lys638Asn
ENST00000529993.5:c.*520G>T	ENSP00000436652.1:n.*520G>T
NM_001291902.1:c.171G>T	NP_001278831.1:p.Lys57Asn
NM_002335.3:c.1914G>T	NP_002326.2:p.Lys638Asn
XM_005273994.2:c.1914G>T	XP_005274051.1:p.Lys638Asn
XM_011545029.1:c.1941G>T	XP_011543331.1:p.Lys647Asn
XM_011545030.1:c.1941G>T	XP_011543332.1:p.Lys647Asn
XM_011545031.1:c.1941G>T	XP_011543333.1:p.Lys647Asn
XR_949925.1:n.1956G>T
XR_949926.1:n.1956G>T
XM_017017735.1:c.171G>T	XP_016873224.1:p.Lys57Asn
XR_001747874.1:n.1956G>T
XR_949925.2:n.1956G>T
XR_949926.2:n.1956G>T
NM_002335.4:c.1914G>T MANE Select	NP_002326.2:p.Lys638Asn
NM_001291902.2:c.171G>T	NP_001278831.1:p.Lys57Asn