Canonical Allele Identifier: CA381618282
Gene: LRP5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68413745T>A , CM000673.2:g.68413745T>A GRCh38
NC_000011.9:g.68181213T>A , CM000673.1:g.68181213T>A GRCh37
NC_000011.8:g.67937789T>A NCBI36
NG_015835.1:g.106106T>A
NG_015835.2:g.106106T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000294304.12:c.2560T>A MANE Select ENSP00000294304.6:p.Tyr854Asn
ENST00000294304.11:c.2560T>A ENSP00000294304.6:p.Tyr854Asn
ENST00000529993.5:c.*1166T>A ENSP00000436652.1:n.*1166T>A
NM_001291902.1:c.817T>A NP_001278831.1:p.Tyr273Asn
NM_002335.3:c.2560T>A NP_002326.2:p.Tyr854Asn
XM_005273994.2:c.2560T>A XP_005274051.1:p.Tyr854Asn
XM_011545029.1:c.2587T>A XP_011543331.1:p.Tyr863Asn
XM_011545030.1:c.2587T>A XP_011543332.1:p.Tyr863Asn
XM_011545031.1:c.2587T>A XP_011543333.1:p.Tyr863Asn
XR_949925.1:n.2602T>A
XR_949926.1:n.2602T>A
XM_017017735.1:c.817T>A XP_016873224.1:p.Tyr273Asn
XM_017017736.1:c.100T>A XP_016873225.1:p.Tyr34Asn
XR_001747874.1:n.2826T>A
XR_949925.2:n.2602T>A
XR_949926.2:n.2602T>A
NM_002335.4:c.2560T>A MANE Select NP_002326.2:p.Tyr854Asn
NM_001291902.2:c.817T>A NP_001278831.1:p.Tyr273Asn