Canonical Allele Identifier: CA1981828423

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080620A= , CM000673.2:g.72080620A= GRCh38
NC_000011.9:g.71791666A= , CM000673.1:g.71791666A= GRCh37
NC_000011.8:g.71469314A= NCBI36
NG_021423.1:g.5285A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-405A= (LRRC51) ENSP00000289488.2:n.-405A=
ENST00000535883.6:c.-282A= (LRRC51) ENSP00000437561.1:n.-282A=
ENST00000538413.6:c.-321A= (LRRC51) ENSP00000438762.2:n.-321A=
ENST00000539271.6:c.-475A= (LRRC51) ENSP00000442267.2:n.-475A=
ENST00000642648.1:c.-282A= (LRRC51) ENSP00000494362.1:n.-282A=
ENST00000642813.1:n.55A= (LRRC51)
ENST00000647530.1:c.-568A= (LRRC51) ENSP00000494072.1:n.-568A=
ENST00000307198.11:c.-587A= (LRRC51) ENSP00000305742.7:n.-587A=
ENST00000393695.7:c.-265T= (NUMA1) ENSP00000377298.3:n.-265T=
ENST00000535883.5:c.-405A= (LRRC51) ENSP00000437561.1:n.-405A=
ENST00000538413.5:c.-282A= (LRRC51) ENSP00000438762.1:n.-282A=
ENST00000543450.1:n.74T= (NUMA1)
ENST00000613205.4:c.-265T= (NUMA1) ENSP00000480172.1:n.-265T=
NM_001145307.4:c.-405A= (LRTOMT) NP_001138779.1:n.-405A=
NM_001145308.4:c.-587A= (LRTOMT) NP_001138780.1:n.-587A=
NM_001145309.3:c.-808A= (LRTOMT) NP_001138781.1:n.-808A=
NM_001145310.3:c.-808A= (LRTOMT) NP_001138782.1:n.-808A=
NM_001205138.3:c.-322A= (LRTOMT) NP_001192067.1:n.-322A=
NM_001271471.2:c.-405A= (LRTOMT) NP_001258400.1:n.-405A=
NM_001286561.1:c.-363T= (NUMA1) NP_001273490.1:n.-363T=
NM_006185.3:c.-265T= (NUMA1) NP_006176.2:n.-265T=
NM_145309.5:c.-405A= (LRTOMT) NP_660352.1:n.-405A=
NR_026886.3:n.290A= (LRTOMT)
XM_011545055.1:c.-265T= (NUMA1) XP_011543357.1:n.-265T=
NM_001318803.1:c.-362A= (LRTOMT) NP_001305732.1:n.-362A=
NR_134858.1:n.290A= (LRTOMT)
XM_006718474.4:c.-321A= (LRTOMT) XP_006718537.1:n.-321A=
XM_011544848.3:c.-568A= (LRTOMT) XP_011543150.1:n.-568A=