Canonical Allele Identifier: CA654520403

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080681dup , CM000673.2:g.72080681dup GRCh38
NC_000011.9:g.71791727dup , CM000673.1:g.71791727dup GRCh37
NC_000011.8:g.71469375dup NCBI36
NG_021423.1:g.5346dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-344dup (LRRC51) ENSP00000289488.2:n.-344dup
ENST00000535883.6:c.-221dup (LRRC51) ENSP00000437561.1:n.-221dup
ENST00000538413.6:c.-260dup (LRRC51) ENSP00000438762.2:n.-260dup
ENST00000539271.6:c.-414dup (LRRC51) ENSP00000442267.2:n.-414dup
ENST00000642510.1:c.-537dup (LRRC51) ENSP00000496544.1:n.-537dup
ENST00000642648.1:c.-221dup (LRRC51) ENSP00000494362.1:n.-221dup
ENST00000642813.1:n.116dup (LRRC51)
ENST00000647530.1:c.-507dup (LRRC51) ENSP00000494072.1:n.-507dup
ENST00000289488.6:c.-344dup (LRRC51) ENSP00000289488.2:n.-344dup
ENST00000307198.11:c.-526dup (LRRC51) ENSP00000305742.7:n.-526dup
ENST00000393695.7:c.-326dup (NUMA1) ENSP00000377298.3:n.-326dup
ENST00000535883.5:c.-344dup (LRRC51) ENSP00000437561.1:n.-344dup
ENST00000538413.5:c.-221dup (LRRC51) ENSP00000438762.1:n.-221dup
ENST00000543450.1:n.13dup (NUMA1)
ENST00000613205.4:c.-326dup (NUMA1) ENSP00000480172.1:n.-326dup
NM_001145307.4:c.-344dup (LRTOMT) NP_001138779.1:n.-344dup
NM_001145308.4:c.-526dup (LRTOMT) NP_001138780.1:n.-526dup
NM_001145309.3:c.-747dup (LRTOMT) NP_001138781.1:n.-747dup
NM_001145310.3:c.-747dup (LRTOMT) NP_001138782.1:n.-747dup
NM_001205138.3:c.-261dup (LRTOMT) NP_001192067.1:n.-261dup
NM_001271471.2:c.-344dup (LRTOMT) NP_001258400.1:n.-344dup
NM_001286561.1:c.-424dup (NUMA1) NP_001273490.1:n.-424dup
NM_006185.3:c.-326dup (NUMA1) NP_006176.2:n.-326dup
NM_145309.5:c.-344dup (LRTOMT) NP_660352.1:n.-344dup
NR_026886.3:n.351dup (LRTOMT)
XM_006718473.2:c.-221dup (LRTOMT) XP_006718536.1:n.-221dup
XM_011545055.1:c.-326dup (NUMA1) XP_011543357.1:n.-326dup
NM_001318803.1:c.-301dup (LRTOMT) NP_001305732.1:n.-301dup
NR_134858.1:n.351dup (LRTOMT)
XM_006718473.4:c.-221dup (LRTOMT) XP_006718536.1:n.-221dup
XM_006718474.4:c.-260dup (LRTOMT) XP_006718537.1:n.-260dup
XM_011544848.3:c.-507dup (LRTOMT) XP_011543150.1:n.-507dup