Canonical Allele Identifier: CA1981828416

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080597C= , CM000673.2:g.72080597C= GRCh38
NC_000011.9:g.71791643C= , CM000673.1:g.71791643C= GRCh37
NC_000011.8:g.71469291C= NCBI36
NG_021423.1:g.5262C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-428C= (LRRC51) ENSP00000289488.2:n.-428C=
ENST00000535883.6:c.-305C= (LRRC51) ENSP00000437561.1:n.-305C=
ENST00000538413.6:c.-344C= (LRRC51) ENSP00000438762.2:n.-344C=
ENST00000642648.1:c.-305C= (LRRC51) ENSP00000494362.1:n.-305C=
ENST00000642813.1:n.32C= (LRRC51)
ENST00000647530.1:c.-591C= (LRRC51) ENSP00000494072.1:n.-591C=
ENST00000307198.11:c.-610C= (LRRC51) ENSP00000305742.7:n.-610C=
ENST00000393695.7:c.-242G= (NUMA1) ENSP00000377298.3:n.-242G=
ENST00000535883.5:c.-428C= (LRRC51) ENSP00000437561.1:n.-428C=
ENST00000538413.5:c.-305C= (LRRC51) ENSP00000438762.1:n.-305C=
ENST00000543450.1:n.97G= (NUMA1)
ENST00000613205.4:c.-242G= (NUMA1) ENSP00000480172.1:n.-242G=
NM_001145307.4:c.-428C= (LRTOMT) NP_001138779.1:n.-428C=
NM_001145308.4:c.-610C= (LRTOMT) NP_001138780.1:n.-610C=
NM_001145309.3:c.-831C= (LRTOMT) NP_001138781.1:n.-831C=
NM_001145310.3:c.-831C= (LRTOMT) NP_001138782.1:n.-831C=
NM_001205138.3:c.-345C= (LRTOMT) NP_001192067.1:n.-345C=
NM_001271471.2:c.-428C= (LRTOMT) NP_001258400.1:n.-428C=
NM_001286561.1:c.-340G= (NUMA1) NP_001273490.1:n.-340G=
NM_006185.3:c.-242G= (NUMA1) NP_006176.2:n.-242G=
NM_145309.5:c.-428C= (LRTOMT) NP_660352.1:n.-428C=
NR_026886.3:n.267C= (LRTOMT)
XM_011545055.1:c.-242G= (NUMA1) XP_011543357.1:n.-242G=
NM_001318803.1:c.-385C= (LRTOMT) NP_001305732.1:n.-385C=
NR_134858.1:n.267C= (LRTOMT)
XM_006718474.4:c.-344C= (LRTOMT) XP_006718537.1:n.-344C=