Canonical Allele Identifier: CA600079858

Linked Data

dbSNP Id: rs1243017559

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080665C>T , CM000673.2:g.72080665C>T GRCh38
NC_000011.9:g.71791711C>T , CM000673.1:g.71791711C>T GRCh37
NC_000011.8:g.71469359C>T NCBI36
NG_021423.1:g.5330C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-360C>T (LRRC51) ENSP00000289488.2:n.-360C>T
ENST00000535883.6:c.-237C>T (LRRC51) ENSP00000437561.1:n.-237C>T
ENST00000538413.6:c.-276C>T (LRRC51) ENSP00000438762.2:n.-276C>T
ENST00000539271.6:c.-430C>T (LRRC51) ENSP00000442267.2:n.-430C>T
ENST00000642648.1:c.-237C>T (LRRC51) ENSP00000494362.1:n.-237C>T
ENST00000642813.1:n.100C>T (LRRC51)
ENST00000647530.1:c.-523C>T (LRRC51) ENSP00000494072.1:n.-523C>T
ENST00000289488.6:c.-360C>T (LRRC51) ENSP00000289488.2:n.-360C>T
ENST00000307198.11:c.-542C>T (LRRC51) ENSP00000305742.7:n.-542C>T
ENST00000393695.7:c.-310G>A (NUMA1) ENSP00000377298.3:n.-310G>A
ENST00000535883.5:c.-360C>T (LRRC51) ENSP00000437561.1:n.-360C>T
ENST00000538413.5:c.-237C>T (LRRC51) ENSP00000438762.1:n.-237C>T
ENST00000543450.1:n.29G>A (NUMA1)
ENST00000613205.4:c.-310G>A (NUMA1) ENSP00000480172.1:n.-310G>A
NM_001145307.4:c.-360C>T (LRTOMT) NP_001138779.1:n.-360C>T
NM_001145308.4:c.-542C>T (LRTOMT) NP_001138780.1:n.-542C>T
NM_001145309.3:c.-763C>T (LRTOMT) NP_001138781.1:n.-763C>T
NM_001145310.3:c.-763C>T (LRTOMT) NP_001138782.1:n.-763C>T
NM_001205138.3:c.-277C>T (LRTOMT) NP_001192067.1:n.-277C>T
NM_001271471.2:c.-360C>T (LRTOMT) NP_001258400.1:n.-360C>T
NM_001286561.1:c.-408G>A (NUMA1) NP_001273490.1:n.-408G>A
NM_006185.3:c.-310G>A (NUMA1) NP_006176.2:n.-310G>A
NM_145309.5:c.-360C>T (LRTOMT) NP_660352.1:n.-360C>T
NR_026886.3:n.335C>T (LRTOMT)
XM_011545055.1:c.-310G>A (NUMA1) XP_011543357.1:n.-310G>A
NM_001318803.1:c.-317C>T (LRTOMT) NP_001305732.1:n.-317C>T
NR_134858.1:n.335C>T (LRTOMT)
XM_006718474.4:c.-276C>T (LRTOMT) XP_006718537.1:n.-276C>T
XM_011544848.3:c.-523C>T (LRTOMT) XP_011543150.1:n.-523C>T