Canonical Allele Identifier: CA1980629790
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68347965C= , CM000673.2:g.68347965C= GRCh38
NC_000011.9:g.68115433C= , CM000673.1:g.68115433C= GRCh37
NC_000011.8:g.67872009C= NCBI36
NG_015835.1:g.40326C=
NG_015835.2:g.40326C=

Transcript Alleles

HGVS Amino-acid change
ENST00000294304.12:c.210C= MANE Select ENSP00000294304.6:p.Phe70=
ENST00000294304.11:c.210C= ENSP00000294304.6:p.Phe70=
ENST00000529993.5:c.210C= ENSP00000436652.1:p.Phe70=
NM_001291902.1:c.-1556C= NP_001278831.1:n.-1556C=
NM_002335.3:c.210C= NP_002326.2:p.Phe70=
XM_005273994.2:c.210C= XP_005274051.1:p.Phe70=
XM_011545029.1:c.237C= XP_011543331.1:p.Phe79=
XM_011545030.1:c.237C= XP_011543332.1:p.Phe79=
XM_011545031.1:c.237C= XP_011543333.1:p.Phe79=
XR_949925.1:n.252C=
XR_949926.1:n.252C=
XR_001747874.1:n.252C=
XR_949925.2:n.252C=
XR_949926.2:n.252C=
NM_002335.4:c.210C= MANE Select NP_002326.2:p.Phe70=
NM_001291902.2:c.-1556C= NP_001278831.1:n.-1556C=