Canonical Allele Identifier: CA679952764

Linked Data

dbSNP Id: rs1376866255

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080638del , CM000673.2:g.72080638del GRCh38
NC_000011.9:g.71791684del , CM000673.1:g.71791684del GRCh37
NC_000011.8:g.71469332del NCBI36
NG_021423.1:g.5303del

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-387del (LRRC51) ENSP00000289488.2:n.-387del
ENST00000535883.6:c.-264del (LRRC51) ENSP00000437561.1:n.-264del
ENST00000538413.6:c.-303del (LRRC51) ENSP00000438762.2:n.-303del
ENST00000539271.6:c.-457del (LRRC51) ENSP00000442267.2:n.-457del
ENST00000642648.1:c.-264del (LRRC51) ENSP00000494362.1:n.-264del
ENST00000642813.1:n.73del (LRRC51)
ENST00000647530.1:c.-550del (LRRC51) ENSP00000494072.1:n.-550del
ENST00000307198.11:c.-569del (LRRC51) ENSP00000305742.7:n.-569del
ENST00000393695.7:c.-282del (NUMA1) ENSP00000377298.3:n.-282del
ENST00000535883.5:c.-387del (LRRC51) ENSP00000437561.1:n.-387del
ENST00000538413.5:c.-264del (LRRC51) ENSP00000438762.1:n.-264del
ENST00000543450.1:n.57del (NUMA1)
ENST00000613205.4:c.-282del (NUMA1) ENSP00000480172.1:n.-282del
NM_001145307.4:c.-387del (LRTOMT) NP_001138779.1:n.-387del
NM_001145308.4:c.-569del (LRTOMT) NP_001138780.1:n.-569del
NM_001145309.3:c.-790del (LRTOMT) NP_001138781.1:n.-790del
NM_001145310.3:c.-790del (LRTOMT) NP_001138782.1:n.-790del
NM_001205138.3:c.-304del (LRTOMT) NP_001192067.1:n.-304del
NM_001271471.2:c.-387del (LRTOMT) NP_001258400.1:n.-387del
NM_001286561.1:c.-380del (NUMA1) NP_001273490.1:n.-380del
NM_006185.3:c.-282del (NUMA1) NP_006176.2:n.-282del
NM_145309.5:c.-387del (LRTOMT) NP_660352.1:n.-387del
NR_026886.3:n.308del (LRTOMT)
XM_011545055.1:c.-282del (NUMA1) XP_011543357.1:n.-282del
NM_001318803.1:c.-344del (LRTOMT) NP_001305732.1:n.-344del
NR_134858.1:n.308del (LRTOMT)
XM_006718474.4:c.-303del (LRTOMT) XP_006718537.1:n.-303del
XM_011544848.3:c.-550del (LRTOMT) XP_011543150.1:n.-550del