Canonical Allele Identifier: CA2561184693

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080612G>T , CM000673.2:g.72080612G>T GRCh38
NC_000011.9:g.71791658G>T , CM000673.1:g.71791658G>T GRCh37
NC_000011.8:g.71469306G>T NCBI36
NG_021423.1:g.5277G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-413G>T (LRRC51) ENSP00000289488.2:n.-413G>T
ENST00000535883.6:c.-290G>T (LRRC51) ENSP00000437561.1:n.-290G>T
ENST00000538413.6:c.-329G>T (LRRC51) ENSP00000438762.2:n.-329G>T
ENST00000539271.6:c.-483G>T (LRRC51) ENSP00000442267.2:n.-483G>T
ENST00000642648.1:c.-290G>T (LRRC51) ENSP00000494362.1:n.-290G>T
ENST00000642813.1:n.47G>T (LRRC51)
ENST00000647530.1:c.-576G>T (LRRC51) ENSP00000494072.1:n.-576G>T
ENST00000307198.11:c.-595G>T (LRRC51) ENSP00000305742.7:n.-595G>T
ENST00000393695.7:c.-257C>A (NUMA1) ENSP00000377298.3:n.-257C>A
ENST00000535883.5:c.-413G>T (LRRC51) ENSP00000437561.1:n.-413G>T
ENST00000538413.5:c.-290G>T (LRRC51) ENSP00000438762.1:n.-290G>T
ENST00000543450.1:n.82C>A (NUMA1)
ENST00000613205.4:c.-257C>A (NUMA1) ENSP00000480172.1:n.-257C>A
NM_001145307.4:c.-413G>T (LRTOMT) NP_001138779.1:n.-413G>T
NM_001145308.4:c.-595G>T (LRTOMT) NP_001138780.1:n.-595G>T
NM_001145309.3:c.-816G>T (LRTOMT) NP_001138781.1:n.-816G>T
NM_001145310.3:c.-816G>T (LRTOMT) NP_001138782.1:n.-816G>T
NM_001205138.3:c.-330G>T (LRTOMT) NP_001192067.1:n.-330G>T
NM_001271471.2:c.-413G>T (LRTOMT) NP_001258400.1:n.-413G>T
NM_001286561.1:c.-355C>A (NUMA1) NP_001273490.1:n.-355C>A
NM_006185.3:c.-257C>A (NUMA1) NP_006176.2:n.-257C>A
NM_145309.5:c.-413G>T (LRTOMT) NP_660352.1:n.-413G>T
NR_026886.3:n.282G>T (LRTOMT)
XM_011545055.1:c.-257C>A (NUMA1) XP_011543357.1:n.-257C>A
NM_001318803.1:c.-370G>T (LRTOMT) NP_001305732.1:n.-370G>T
NR_134858.1:n.282G>T (LRTOMT)
XM_006718474.4:c.-329G>T (LRTOMT) XP_006718537.1:n.-329G>T
XM_011544848.3:c.-576G>T (LRTOMT) XP_011543150.1:n.-576G>T