Canonical Allele Identifier: CA381615424
Gene: LRP5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68406573C>G , CM000673.2:g.68406573C>G GRCh38
NC_000011.9:g.68174041C>G , CM000673.1:g.68174041C>G GRCh37
NC_000011.8:g.67930617C>G NCBI36
NG_015835.1:g.98934C>G
NG_015835.2:g.98934C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.1851C>G MANE Select ENSP00000294304.6:p.Phe617Leu
ENST00000294304.11:c.1851C>G ENSP00000294304.6:p.Phe617Leu
ENST00000529993.5:c.*457C>G ENSP00000436652.1:n.*457C>G
NM_001291902.1:c.108C>G NP_001278831.1:p.Phe36Leu
NM_002335.3:c.1851C>G NP_002326.2:p.Phe617Leu
XM_005273994.2:c.1851C>G XP_005274051.1:p.Phe617Leu
XM_011545029.1:c.1878C>G XP_011543331.1:p.Phe626Leu
XM_011545030.1:c.1878C>G XP_011543332.1:p.Phe626Leu
XM_011545031.1:c.1878C>G XP_011543333.1:p.Phe626Leu
XR_949925.1:n.1893C>G
XR_949926.1:n.1893C>G
XM_017017735.1:c.108C>G XP_016873224.1:p.Phe36Leu
XR_001747874.1:n.1893C>G
XR_949925.2:n.1893C>G
XR_949926.2:n.1893C>G
NM_002335.4:c.1851C>G MANE Select NP_002326.2:p.Phe617Leu
NM_001291902.2:c.108C>G NP_001278831.1:p.Phe36Leu