Canonical Allele Identifier: CA2792542478
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68433933_68433936del , CM000673.2:g.68433933_68433936del GRCh38
NC_000011.9:g.68201401_68201404del , CM000673.1:g.68201401_68201404del GRCh37
NC_000011.8:g.67957977_67957980del NCBI36
NG_015835.1:g.126294_126297del
NG_015835.2:g.126294_126297del

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.4000+95_4000+98del MANE Select ENSP00000294304.6:n.4000+95_4000+98del
ENST00000294304.11:c.4000+95_4000+98del ENSP00000294304.6:n.4000+95_4000+98del
ENST00000529993.5:c.*2606+95_*2606+98del ENSP00000436652.1:n.*2606+95_*2606+98del
NM_001291902.1:c.2257+95_2257+98del NP_001278831.1:n.2257+95_2257+98del
NM_002335.3:c.4000+95_4000+98del NP_002326.2:n.4000+95_4000+98del
XM_005273994.2:c.4000+95_4000+98del XP_005274051.1:n.4000+95_4000+98del
XM_011545029.1:c.4027+95_4027+98del XP_011543331.1:n.4027+95_4027+98del
XM_011545030.1:c.4027+95_4027+98del XP_011543332.1:n.4027+95_4027+98del
XM_011545031.1:c.4027+95_4027+98del XP_011543333.1:n.4027+95_4027+98del
XR_949925.1:n.4042+95_4042+98del
XR_949926.1:n.4042+95_4042+98del
XM_017017735.1:c.2257+95_2257+98del XP_016873224.1:n.2257+95_2257+98del
XM_017017736.1:c.1540+95_1540+98del XP_016873225.1:n.1540+95_1540+98del
XR_949925.2:n.4042+95_4042+98del
XR_949926.2:n.4042+95_4042+98del
NM_002335.4:c.4000+95_4000+98del MANE Select NP_002326.2:n.4000+95_4000+98del
NM_001291902.2:c.2257+95_2257+98del NP_001278831.1:n.2257+95_2257+98del