Canonical Allele Identifier: CA1980651587
Community Standard Title: NM_002335.4(LRP5):c.1648G= (p.Gly550=)
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68403546G= , CM000673.2:g.68403546G= GRCh38
NC_000011.9:g.68171014G= , CM000673.1:g.68171014G= GRCh37
NC_000011.8:g.67927590G= NCBI36
NG_015835.1:g.95907G=
NG_015835.2:g.95907G=

Transcript Alleles

HGVS Amino-acid Change
NM_002335.4:c.1648G= MANE Select NP_002326.2:p.Gly550=
ENST00000294304.12:c.1648G= MANE Select ENSP00000294304.6:p.Gly550=
NM_001291902.1:c.-290G= NP_001278831.1:n.-290G=
NM_001291902.2:c.-290G= NP_001278831.1:n.-290G=
NM_002335.3:c.1648G= NP_002326.2:p.Gly550=
ENST00000294304.11:c.1648G= ENSP00000294304.6:p.Gly550=
ENST00000529993.5:c.*60G= ENSP00000436652.1:n.*60G=
XM_005273994.2:c.1648G= XP_005274051.1:p.Gly550=
XM_011545029.1:c.1675G= XP_011543331.1:p.Gly559=
XM_011545030.1:c.1675G= XP_011543332.1:p.Gly559=
XM_011545031.1:c.1675G= XP_011543333.1:p.Gly559=
XR_001747874.1:n.1690G=
XR_949925.1:n.1690G=
XR_949925.2:n.1690G=
XR_949926.1:n.1690G=
XR_949926.2:n.1690G=