Canonical Allele Identifier: CA1980622666
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68433848_68433849delinsTC , CM000673.2:g.68433848_68433849delinsTC GRCh38
NC_000011.9:g.68201316_68201317delinsTC , CM000673.1:g.68201316_68201317delinsTC GRCh37
NC_000011.8:g.67957892_67957893delinsTC NCBI36
NG_015835.1:g.126209_126210delinsTC
NG_015835.2:g.126209_126210delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.4000+10_4000+11delinsTC MANE Select ENSP00000294304.6:n.4000+10_4000+11delinsTC
ENST00000294304.11:c.4000+10_4000+11delinsTC ENSP00000294304.6:n.4000+10_4000+11delinsTC
ENST00000529993.5:c.*2606+10_*2606+11delinsTC ENSP00000436652.1:n.*2606+10_*2606+11delinsTC
NM_001291902.1:c.2257+10_2257+11delinsTC NP_001278831.1:n.2257+10_2257+11delinsTC
NM_002335.3:c.4000+10_4000+11delinsTC NP_002326.2:n.4000+10_4000+11delinsTC
XM_005273994.2:c.4000+10_4000+11delinsTC XP_005274051.1:n.4000+10_4000+11delinsTC
XM_011545029.1:c.4027+10_4027+11delinsTC XP_011543331.1:n.4027+10_4027+11delinsTC
XM_011545030.1:c.4027+10_4027+11delinsTC XP_011543332.1:n.4027+10_4027+11delinsTC
XM_011545031.1:c.4027+10_4027+11delinsTC XP_011543333.1:n.4027+10_4027+11delinsTC
XR_949925.1:n.4042+10_4042+11delinsTC
XR_949926.1:n.4042+10_4042+11delinsTC
XM_017017735.1:c.2257+10_2257+11delinsTC XP_016873224.1:n.2257+10_2257+11delinsTC
XM_017017736.1:c.1540+10_1540+11delinsTC XP_016873225.1:n.1540+10_1540+11delinsTC
XR_949925.2:n.4042+10_4042+11delinsTC
XR_949926.2:n.4042+10_4042+11delinsTC
NM_002335.4:c.4000+10_4000+11delinsTC MANE Select NP_002326.2:n.4000+10_4000+11delinsTC
NM_001291902.2:c.2257+10_2257+11delinsTC NP_001278831.1:n.2257+10_2257+11delinsTC