Canonical Allele Identifier: CA381613639
Gene: LRP5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68433635G>T , CM000673.2:g.68433635G>T GRCh38
NC_000011.9:g.68201103G>T , CM000673.1:g.68201103G>T GRCh37
NC_000011.8:g.67957679G>T NCBI36
NG_015835.1:g.125996G>T
NG_015835.2:g.125996G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000294304.12:c.3797G>T MANE Select ENSP00000294304.6:p.Cys1266Phe
ENST00000294304.11:c.3797G>T ENSP00000294304.6:p.Cys1266Phe
ENST00000529993.5:c.*2403G>T ENSP00000436652.1:n.*2403G>T
NM_001291902.1:c.2054G>T NP_001278831.1:p.Cys685Phe
NM_002335.3:c.3797G>T NP_002326.2:p.Cys1266Phe
XM_005273994.2:c.3797G>T XP_005274051.1:p.Cys1266Phe
XM_011545029.1:c.3824G>T XP_011543331.1:p.Cys1275Phe
XM_011545030.1:c.3824G>T XP_011543332.1:p.Cys1275Phe
XM_011545031.1:c.3824G>T XP_011543333.1:p.Cys1275Phe
XR_949925.1:n.3839G>T
XR_949926.1:n.3839G>T
XM_017017735.1:c.2054G>T XP_016873224.1:p.Cys685Phe
XM_017017736.1:c.1337G>T XP_016873225.1:p.Cys446Phe
XR_949925.2:n.3839G>T
XR_949926.2:n.3839G>T
NM_002335.4:c.3797G>T MANE Select NP_002326.2:p.Cys1266Phe
NM_001291902.2:c.2054G>T NP_001278831.1:p.Cys685Phe