Canonical Allele Identifier: CA1981828457

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080679C= , CM000673.2:g.72080679C= GRCh38
NC_000011.9:g.71791725C= , CM000673.1:g.71791725C= GRCh37
NC_000011.8:g.71469373C= NCBI36
NG_021423.1:g.5344C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-346C= (LRRC51) ENSP00000289488.2:n.-346C=
ENST00000535883.6:c.-223C= (LRRC51) ENSP00000437561.1:n.-223C=
ENST00000538413.6:c.-262C= (LRRC51) ENSP00000438762.2:n.-262C=
ENST00000539271.6:c.-416C= (LRRC51) ENSP00000442267.2:n.-416C=
ENST00000642510.1:c.-539C= (LRRC51) ENSP00000496544.1:n.-539C=
ENST00000642648.1:c.-223C= (LRRC51) ENSP00000494362.1:n.-223C=
ENST00000642813.1:n.114C= (LRRC51)
ENST00000647530.1:c.-509C= (LRRC51) ENSP00000494072.1:n.-509C=
ENST00000289488.6:c.-346C= (LRRC51) ENSP00000289488.2:n.-346C=
ENST00000307198.11:c.-528C= (LRRC51) ENSP00000305742.7:n.-528C=
ENST00000393695.7:c.-324G= (NUMA1) ENSP00000377298.3:n.-324G=
ENST00000535883.5:c.-346C= (LRRC51) ENSP00000437561.1:n.-346C=
ENST00000538413.5:c.-223C= (LRRC51) ENSP00000438762.1:n.-223C=
ENST00000543450.1:n.15G= (NUMA1)
ENST00000613205.4:c.-324G= (NUMA1) ENSP00000480172.1:n.-324G=
NM_001145307.4:c.-346C= (LRTOMT) NP_001138779.1:n.-346C=
NM_001145308.4:c.-528C= (LRTOMT) NP_001138780.1:n.-528C=
NM_001145309.3:c.-749C= (LRTOMT) NP_001138781.1:n.-749C=
NM_001145310.3:c.-749C= (LRTOMT) NP_001138782.1:n.-749C=
NM_001205138.3:c.-263C= (LRTOMT) NP_001192067.1:n.-263C=
NM_001271471.2:c.-346C= (LRTOMT) NP_001258400.1:n.-346C=
NM_001286561.1:c.-422G= (NUMA1) NP_001273490.1:n.-422G=
NM_006185.3:c.-324G= (NUMA1) NP_006176.2:n.-324G=
NM_145309.5:c.-346C= (LRTOMT) NP_660352.1:n.-346C=
NR_026886.3:n.349C= (LRTOMT)
XM_006718473.2:c.-223C= (LRTOMT) XP_006718536.1:n.-223C=
XM_011545055.1:c.-324G= (NUMA1) XP_011543357.1:n.-324G=
NM_001318803.1:c.-303C= (LRTOMT) NP_001305732.1:n.-303C=
NR_134858.1:n.349C= (LRTOMT)
XM_006718473.4:c.-223C= (LRTOMT) XP_006718536.1:n.-223C=
XM_006718474.4:c.-262C= (LRTOMT) XP_006718537.1:n.-262C=
XM_011544848.3:c.-509C= (LRTOMT) XP_011543150.1:n.-509C=