Canonical Allele Identifier: CA679952851

Linked Data

dbSNP Id: rs1184657338

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080692G>T , CM000673.2:g.72080692G>T GRCh38
NC_000011.9:g.71791738G>T , CM000673.1:g.71791738G>T GRCh37
NC_000011.8:g.71469386G>T NCBI36
NG_021423.1:g.5357G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-333G>T (LRRC51) ENSP00000289488.2:n.-333G>T
ENST00000535883.6:c.-210G>T (LRRC51) ENSP00000437561.1:n.-210G>T
ENST00000538413.6:c.-249G>T (LRRC51) ENSP00000438762.2:n.-249G>T
ENST00000539271.6:c.-403G>T (LRRC51) ENSP00000442267.2:n.-403G>T
ENST00000642510.1:c.-526G>T (LRRC51) ENSP00000496544.1:n.-526G>T
ENST00000642648.1:c.-210G>T (LRRC51) ENSP00000494362.1:n.-210G>T
ENST00000642813.1:n.127G>T (LRRC51)
ENST00000647530.1:c.-496G>T (LRRC51) ENSP00000494072.1:n.-496G>T
ENST00000289488.6:c.-333G>T (LRRC51) ENSP00000289488.2:n.-333G>T
ENST00000307198.11:c.-515G>T (LRRC51) ENSP00000305742.7:n.-515G>T
ENST00000535883.5:c.-333G>T (LRRC51) ENSP00000437561.1:n.-333G>T
ENST00000538413.5:c.-210G>T (LRRC51) ENSP00000438762.1:n.-210G>T
ENST00000543450.1:n.2C>A (NUMA1)
ENST00000613205.4:c.-337C>A (NUMA1) ENSP00000480172.1:n.-337C>A
NM_001145307.4:c.-333G>T (LRTOMT) NP_001138779.1:n.-333G>T
NM_001145308.4:c.-515G>T (LRTOMT) NP_001138780.1:n.-515G>T
NM_001145309.3:c.-736G>T (LRTOMT) NP_001138781.1:n.-736G>T
NM_001145310.3:c.-736G>T (LRTOMT) NP_001138782.1:n.-736G>T
NM_001205138.3:c.-250G>T (LRTOMT) NP_001192067.1:n.-250G>T
NM_001271471.2:c.-333G>T (LRTOMT) NP_001258400.1:n.-333G>T
NM_001286561.1:c.-435C>A (NUMA1) NP_001273490.1:n.-435C>A
NM_006185.3:c.-337C>A (NUMA1) NP_006176.2:n.-337C>A
NM_145309.5:c.-333G>T (LRTOMT) NP_660352.1:n.-333G>T
NR_026886.3:n.362G>T (LRTOMT)
XM_006718473.2:c.-210G>T (LRTOMT) XP_006718536.1:n.-210G>T
NM_001318803.1:c.-290G>T (LRTOMT) NP_001305732.1:n.-290G>T
NR_134858.1:n.362G>T (LRTOMT)
XM_006718473.4:c.-210G>T (LRTOMT) XP_006718536.1:n.-210G>T
XM_006718474.4:c.-249G>T (LRTOMT) XP_006718537.1:n.-249G>T
XM_011544848.3:c.-496G>T (LRTOMT) XP_011543150.1:n.-496G>T