Canonical Allele Identifier: CA1980651752
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68403615A= , CM000673.2:g.68403615A= GRCh38
NC_000011.9:g.68171083A= , CM000673.1:g.68171083A= GRCh37
NC_000011.8:g.67927659A= NCBI36
NG_015835.1:g.95976A=
NG_015835.2:g.95976A=

Transcript Alleles

HGVS Amino-acid change
ENST00000294304.12:c.1717A= MANE Select ENSP00000294304.6:p.Lys573=
ENST00000294304.11:c.1717A= ENSP00000294304.6:p.Lys573=
ENST00000529993.5:c.*129A= ENSP00000436652.1:n.*129A=
NM_001291902.1:c.-221A= NP_001278831.1:n.-221A=
NM_002335.3:c.1717A= NP_002326.2:p.Lys573=
XM_005273994.2:c.1717A= XP_005274051.1:p.Lys573=
XM_011545029.1:c.1744A= XP_011543331.1:p.Lys582=
XM_011545030.1:c.1744A= XP_011543332.1:p.Lys582=
XM_011545031.1:c.1744A= XP_011543333.1:p.Lys582=
XR_949925.1:n.1759A=
XR_949926.1:n.1759A=
XR_001747874.1:n.1759A=
XR_949925.2:n.1759A=
XR_949926.2:n.1759A=
NM_002335.4:c.1717A= MANE Select NP_002326.2:p.Lys573=
NM_001291902.2:c.-221A= NP_001278831.1:n.-221A=