Canonical Allele Identifier: CA939427127

Linked Data

dbSNP Id: rs1944098125

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080650G>A , CM000673.2:g.72080650G>A GRCh38
NC_000011.9:g.71791696G>A , CM000673.1:g.71791696G>A GRCh37
NC_000011.8:g.71469344G>A NCBI36
NG_021423.1:g.5315G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-375G>A (LRRC51) ENSP00000289488.2:n.-375G>A
ENST00000535883.6:c.-252G>A (LRRC51) ENSP00000437561.1:n.-252G>A
ENST00000538413.6:c.-291G>A (LRRC51) ENSP00000438762.2:n.-291G>A
ENST00000539271.6:c.-445G>A (LRRC51) ENSP00000442267.2:n.-445G>A
ENST00000642648.1:c.-252G>A (LRRC51) ENSP00000494362.1:n.-252G>A
ENST00000642813.1:n.85G>A (LRRC51)
ENST00000647530.1:c.-538G>A (LRRC51) ENSP00000494072.1:n.-538G>A
ENST00000289488.6:c.-375G>A (LRRC51) ENSP00000289488.2:n.-375G>A
ENST00000307198.11:c.-557G>A (LRRC51) ENSP00000305742.7:n.-557G>A
ENST00000393695.7:c.-295C>T (NUMA1) ENSP00000377298.3:n.-295C>T
ENST00000535883.5:c.-375G>A (LRRC51) ENSP00000437561.1:n.-375G>A
ENST00000538413.5:c.-252G>A (LRRC51) ENSP00000438762.1:n.-252G>A
ENST00000543450.1:n.44C>T (NUMA1)
ENST00000613205.4:c.-295C>T (NUMA1) ENSP00000480172.1:n.-295C>T
NM_001145307.4:c.-375G>A (LRTOMT) NP_001138779.1:n.-375G>A
NM_001145308.4:c.-557G>A (LRTOMT) NP_001138780.1:n.-557G>A
NM_001145309.3:c.-778G>A (LRTOMT) NP_001138781.1:n.-778G>A
NM_001145310.3:c.-778G>A (LRTOMT) NP_001138782.1:n.-778G>A
NM_001205138.3:c.-292G>A (LRTOMT) NP_001192067.1:n.-292G>A
NM_001271471.2:c.-375G>A (LRTOMT) NP_001258400.1:n.-375G>A
NM_001286561.1:c.-393C>T (NUMA1) NP_001273490.1:n.-393C>T
NM_006185.3:c.-295C>T (NUMA1) NP_006176.2:n.-295C>T
NM_145309.5:c.-375G>A (LRTOMT) NP_660352.1:n.-375G>A
NR_026886.3:n.320G>A (LRTOMT)
XM_011545055.1:c.-295C>T (NUMA1) XP_011543357.1:n.-295C>T
NM_001318803.1:c.-332G>A (LRTOMT) NP_001305732.1:n.-332G>A
NR_134858.1:n.320G>A (LRTOMT)
XM_006718474.4:c.-291G>A (LRTOMT) XP_006718537.1:n.-291G>A
XM_011544848.3:c.-538G>A (LRTOMT) XP_011543150.1:n.-538G>A