Canonical Allele Identifier: CA2792540625
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68410207_68410209del , CM000673.2:g.68410207_68410209del GRCh38
NC_000011.9:g.68177675_68177677del , CM000673.1:g.68177675_68177677del GRCh37
NC_000011.8:g.67934251_67934253del NCBI36
NG_015835.1:g.102568_102570del
NG_015835.2:g.102568_102570del

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.2318+67_2318+69del MANE Select ENSP00000294304.6:n.2318+67_2318+69del
ENST00000294304.11:c.2318+67_2318+69del ENSP00000294304.6:n.2318+67_2318+69del
ENST00000528714.1:n.112+67_112+69del
ENST00000529993.5:c.*924+67_*924+69del ENSP00000436652.1:n.*924+67_*924+69del
NM_001291902.1:c.575+67_575+69del NP_001278831.1:n.575+67_575+69del
NM_002335.3:c.2318+67_2318+69del NP_002326.2:n.2318+67_2318+69del
XM_005273994.2:c.2318+67_2318+69del XP_005274051.1:n.2318+67_2318+69del
XM_011545029.1:c.2345+67_2345+69del XP_011543331.1:n.2345+67_2345+69del
XM_011545030.1:c.2345+67_2345+69del XP_011543332.1:n.2345+67_2345+69del
XM_011545031.1:c.2345+67_2345+69del XP_011543333.1:n.2345+67_2345+69del
XR_949925.1:n.2360+67_2360+69del
XR_949926.1:n.2360+67_2360+69del
XM_017017735.1:c.575+67_575+69del XP_016873224.1:n.575+67_575+69del
XR_001747874.1:n.2360+67_2360+69del
XR_949925.2:n.2360+67_2360+69del
XR_949926.2:n.2360+67_2360+69del
NM_002335.4:c.2318+67_2318+69del MANE Select NP_002326.2:n.2318+67_2318+69del
NM_001291902.2:c.575+67_575+69del NP_001278831.1:n.575+67_575+69del