Canonical Allele Identifier: CA1980639669
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68357675G= , CM000673.2:g.68357675G= GRCh38
NC_000011.9:g.68125143G= , CM000673.1:g.68125143G= GRCh37
NC_000011.8:g.67881719G= NCBI36
NG_015835.1:g.50036G=
NG_015835.2:g.50036G=

Transcript Alleles

HGVS Amino-acid change
ENST00000294304.12:c.514G= MANE Select ENSP00000294304.6:p.Glu172=
ENST00000294304.11:c.514G= ENSP00000294304.6:p.Glu172=
ENST00000529993.5:c.514G= ENSP00000436652.1:p.Glu172=
NM_001291902.1:c.-1252G= NP_001278831.1:n.-1252G=
NM_002335.3:c.514G= NP_002326.2:p.Glu172=
XM_005273994.2:c.514G= XP_005274051.1:p.Glu172=
XM_011545029.1:c.541G= XP_011543331.1:p.Glu181=
XM_011545030.1:c.541G= XP_011543332.1:p.Glu181=
XM_011545031.1:c.541G= XP_011543333.1:p.Glu181=
XR_949925.1:n.556G=
XR_949926.1:n.556G=
XR_001747874.1:n.556G=
XR_949925.2:n.556G=
XR_949926.2:n.556G=
NM_002335.4:c.514G= MANE Select NP_002326.2:p.Glu172=
NM_001291902.2:c.-1252G= NP_001278831.1:n.-1252G=