Canonical Allele Identifier: CA1980651882
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68403696G= , CM000673.2:g.68403696G= GRCh38
NC_000011.9:g.68171164G= , CM000673.1:g.68171164G= GRCh37
NC_000011.8:g.67927740G= NCBI36
NG_015835.1:g.96057G=
NG_015835.2:g.96057G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.1798G= MANE Select ENSP00000294304.6:p.Val600=
ENST00000294304.11:c.1798G= ENSP00000294304.6:p.Val600=
ENST00000529993.5:c.*210G= ENSP00000436652.1:n.*210G=
NM_001291902.1:c.-140G= NP_001278831.1:n.-140G=
NM_002335.3:c.1798G= NP_002326.2:p.Val600=
XM_005273994.2:c.1798G= XP_005274051.1:p.Val600=
XM_011545029.1:c.1825G= XP_011543331.1:p.Val609=
XM_011545030.1:c.1825G= XP_011543332.1:p.Val609=
XM_011545031.1:c.1825G= XP_011543333.1:p.Val609=
XR_949925.1:n.1840G=
XR_949926.1:n.1840G=
XR_001747874.1:n.1840G=
XR_949925.2:n.1840G=
XR_949926.2:n.1840G=
NM_002335.4:c.1798G= MANE Select NP_002326.2:p.Val600=
NM_001291902.2:c.-140G= NP_001278831.1:n.-140G=