Canonical Allele Identifier: CA2792647121

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080623dup , CM000673.2:g.72080623dup GRCh38
NC_000011.9:g.71791669dup , CM000673.1:g.71791669dup GRCh37
NC_000011.8:g.71469317dup NCBI36
NG_021423.1:g.5288dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-402dup (LRRC51) ENSP00000289488.2:n.-402dup
ENST00000535883.6:c.-279dup (LRRC51) ENSP00000437561.1:n.-279dup
ENST00000538413.6:c.-318dup (LRRC51) ENSP00000438762.2:n.-318dup
ENST00000539271.6:c.-472dup (LRRC51) ENSP00000442267.2:n.-472dup
ENST00000642648.1:c.-279dup (LRRC51) ENSP00000494362.1:n.-279dup
ENST00000642813.1:n.58dup (LRRC51)
ENST00000647530.1:c.-565dup (LRRC51) ENSP00000494072.1:n.-565dup
ENST00000307198.11:c.-584dup (LRRC51) ENSP00000305742.7:n.-584dup
ENST00000393695.7:c.-265dup (NUMA1) ENSP00000377298.3:n.-265dup
ENST00000535883.5:c.-402dup (LRRC51) ENSP00000437561.1:n.-402dup
ENST00000538413.5:c.-279dup (LRRC51) ENSP00000438762.1:n.-279dup
ENST00000543450.1:n.74dup (NUMA1)
ENST00000613205.4:c.-265dup (NUMA1) ENSP00000480172.1:n.-265dup
NM_001145307.4:c.-402dup (LRTOMT) NP_001138779.1:n.-402dup
NM_001145308.4:c.-584dup (LRTOMT) NP_001138780.1:n.-584dup
NM_001145309.3:c.-805dup (LRTOMT) NP_001138781.1:n.-805dup
NM_001145310.3:c.-805dup (LRTOMT) NP_001138782.1:n.-805dup
NM_001205138.3:c.-319dup (LRTOMT) NP_001192067.1:n.-319dup
NM_001271471.2:c.-402dup (LRTOMT) NP_001258400.1:n.-402dup
NM_001286561.1:c.-363dup (NUMA1) NP_001273490.1:n.-363dup
NM_006185.3:c.-265dup (NUMA1) NP_006176.2:n.-265dup
NM_145309.5:c.-402dup (LRTOMT) NP_660352.1:n.-402dup
NR_026886.3:n.293dup (LRTOMT)
XM_011545055.1:c.-265dup (NUMA1) XP_011543357.1:n.-265dup
NM_001318803.1:c.-359dup (LRTOMT) NP_001305732.1:n.-359dup
NR_134858.1:n.293dup (LRTOMT)
XM_006718474.4:c.-318dup (LRTOMT) XP_006718537.1:n.-318dup
XM_011544848.3:c.-565dup (LRTOMT) XP_011543150.1:n.-565dup