Canonical Allele Identifier: CA1981828421

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080609A= , CM000673.2:g.72080609A= GRCh38
NC_000011.9:g.71791655A= , CM000673.1:g.71791655A= GRCh37
NC_000011.8:g.71469303A= NCBI36
NG_021423.1:g.5274A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-416A= (LRRC51) ENSP00000289488.2:n.-416A=
ENST00000535883.6:c.-293A= (LRRC51) ENSP00000437561.1:n.-293A=
ENST00000538413.6:c.-332A= (LRRC51) ENSP00000438762.2:n.-332A=
ENST00000539271.6:c.-486A= (LRRC51) ENSP00000442267.2:n.-486A=
ENST00000642648.1:c.-293A= (LRRC51) ENSP00000494362.1:n.-293A=
ENST00000642813.1:n.44A= (LRRC51)
ENST00000647530.1:c.-579A= (LRRC51) ENSP00000494072.1:n.-579A=
ENST00000307198.11:c.-598A= (LRRC51) ENSP00000305742.7:n.-598A=
ENST00000393695.7:c.-254T= (NUMA1) ENSP00000377298.3:n.-254T=
ENST00000535883.5:c.-416A= (LRRC51) ENSP00000437561.1:n.-416A=
ENST00000538413.5:c.-293A= (LRRC51) ENSP00000438762.1:n.-293A=
ENST00000543450.1:n.85T= (NUMA1)
ENST00000613205.4:c.-254T= (NUMA1) ENSP00000480172.1:n.-254T=
NM_001145307.4:c.-416A= (LRTOMT) NP_001138779.1:n.-416A=
NM_001145308.4:c.-598A= (LRTOMT) NP_001138780.1:n.-598A=
NM_001145309.3:c.-819A= (LRTOMT) NP_001138781.1:n.-819A=
NM_001145310.3:c.-819A= (LRTOMT) NP_001138782.1:n.-819A=
NM_001205138.3:c.-333A= (LRTOMT) NP_001192067.1:n.-333A=
NM_001271471.2:c.-416A= (LRTOMT) NP_001258400.1:n.-416A=
NM_001286561.1:c.-352T= (NUMA1) NP_001273490.1:n.-352T=
NM_006185.3:c.-254T= (NUMA1) NP_006176.2:n.-254T=
NM_145309.5:c.-416A= (LRTOMT) NP_660352.1:n.-416A=
NR_026886.3:n.279A= (LRTOMT)
XM_011545055.1:c.-254T= (NUMA1) XP_011543357.1:n.-254T=
NM_001318803.1:c.-373A= (LRTOMT) NP_001305732.1:n.-373A=
NR_134858.1:n.279A= (LRTOMT)
XM_006718474.4:c.-332A= (LRTOMT) XP_006718537.1:n.-332A=
XM_011544848.3:c.-579A= (LRTOMT) XP_011543150.1:n.-579A=