Canonical Allele Identifier: CA381616784
Gene: LRP5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68446444C>A , CM000673.2:g.68446444C>A GRCh38
NC_000011.9:g.68213912C>A , CM000673.1:g.68213912C>A GRCh37
NC_000011.8:g.67970488C>A NCBI36
NG_015835.1:g.138805C>A
NG_015835.2:g.138805C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000294304.12:c.4497C>A MANE Select ENSP00000294304.6:p.Asn1499Lys
ENST00000294304.11:c.4497C>A ENSP00000294304.6:p.Asn1499Lys
ENST00000529702.1:c.167C>A
ENST00000529993.5:c.*3103C>A ENSP00000436652.1:n.*3103C>A
NM_001291902.1:c.2754C>A NP_001278831.1:p.Asn918Lys
NM_002335.3:c.4497C>A NP_002326.2:p.Asn1499Lys
XM_005273994.2:c.4611C>A XP_005274051.1:p.Asn1537Lys
XM_011545029.1:c.4638C>A XP_011543331.1:p.Asn1546Lys
XM_011545030.1:c.4524C>A XP_011543332.1:p.Asn1508Lys
XM_011545031.1:c.4654C>A XP_011543333.1:p.Pro1552Thr
XR_949925.1:n.4653C>A
XR_949926.1:n.4669C>A
XM_017017735.1:c.2868C>A XP_016873224.1:p.Asn956Lys
XM_017017736.1:c.2151C>A XP_016873225.1:p.Asn717Lys
XR_949925.2:n.4653C>A
XR_949926.2:n.4669C>A
NM_002335.4:c.4497C>A MANE Select NP_002326.2:p.Asn1499Lys
NM_001291902.2:c.2754C>A NP_001278831.1:p.Asn918Lys