Canonical Allele Identifier: CA1980629795
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68347967A= , CM000673.2:g.68347967A= GRCh38
NC_000011.9:g.68115435A= , CM000673.1:g.68115435A= GRCh37
NC_000011.8:g.67872011A= NCBI36
NG_015835.1:g.40328A=
NG_015835.2:g.40328A=

Transcript Alleles

HGVS Amino-acid change
ENST00000294304.12:c.212A= MANE Select ENSP00000294304.6:p.Gln71=
ENST00000294304.11:c.212A= ENSP00000294304.6:p.Gln71=
ENST00000529993.5:c.212A= ENSP00000436652.1:p.Gln71=
NM_001291902.1:c.-1554A= NP_001278831.1:n.-1554A=
NM_002335.3:c.212A= NP_002326.2:p.Gln71=
XM_005273994.2:c.212A= XP_005274051.1:p.Gln71=
XM_011545029.1:c.239A= XP_011543331.1:p.Gln80=
XM_011545030.1:c.239A= XP_011543332.1:p.Gln80=
XM_011545031.1:c.239A= XP_011543333.1:p.Gln80=
XR_949925.1:n.254A=
XR_949926.1:n.254A=
XR_001747874.1:n.254A=
XR_949925.2:n.254A=
XR_949926.2:n.254A=
NM_002335.4:c.212A= MANE Select NP_002326.2:p.Gln71=
NM_001291902.2:c.-1554A= NP_001278831.1:n.-1554A=