Canonical Allele Identifier: CA1981828415

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080595G= , CM000673.2:g.72080595G= GRCh38
NC_000011.9:g.71791641G= , CM000673.1:g.71791641G= GRCh37
NC_000011.8:g.71469289G= NCBI36
NG_021423.1:g.5260G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-430G= (LRRC51) ENSP00000289488.2:n.-430G=
ENST00000535883.6:c.-307G= (LRRC51) ENSP00000437561.1:n.-307G=
ENST00000538413.6:c.-346G= (LRRC51) ENSP00000438762.2:n.-346G=
ENST00000642648.1:c.-307G= (LRRC51) ENSP00000494362.1:n.-307G=
ENST00000642813.1:n.30G= (LRRC51)
ENST00000647530.1:c.-593G= (LRRC51) ENSP00000494072.1:n.-593G=
ENST00000307198.11:c.-612G= (LRRC51) ENSP00000305742.7:n.-612G=
ENST00000393695.7:c.-240C= (NUMA1) ENSP00000377298.3:n.-240C=
ENST00000535883.5:c.-430G= (LRRC51) ENSP00000437561.1:n.-430G=
ENST00000538413.5:c.-307G= (LRRC51) ENSP00000438762.1:n.-307G=
ENST00000543450.1:n.99C= (NUMA1)
ENST00000613205.4:c.-240C= (NUMA1) ENSP00000480172.1:n.-240C=
NM_001145307.4:c.-430G= (LRTOMT) NP_001138779.1:n.-430G=
NM_001145308.4:c.-612G= (LRTOMT) NP_001138780.1:n.-612G=
NM_001145309.3:c.-833G= (LRTOMT) NP_001138781.1:n.-833G=
NM_001145310.3:c.-833G= (LRTOMT) NP_001138782.1:n.-833G=
NM_001205138.3:c.-347G= (LRTOMT) NP_001192067.1:n.-347G=
NM_001271471.2:c.-430G= (LRTOMT) NP_001258400.1:n.-430G=
NM_001286561.1:c.-338C= (NUMA1) NP_001273490.1:n.-338C=
NM_006185.3:c.-240C= (NUMA1) NP_006176.2:n.-240C=
NM_145309.5:c.-430G= (LRTOMT) NP_660352.1:n.-430G=
NR_026886.3:n.265G= (LRTOMT)
XM_011545055.1:c.-240C= (NUMA1) XP_011543357.1:n.-240C=
NM_001318803.1:c.-387G= (LRTOMT) NP_001305732.1:n.-387G=
NR_134858.1:n.265G= (LRTOMT)
XM_006718474.4:c.-346G= (LRTOMT) XP_006718537.1:n.-346G=