Canonical Allele Identifier: CA2614916507

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080688G>T , CM000673.2:g.72080688G>T GRCh38
NC_000011.9:g.71791734G>T , CM000673.1:g.71791734G>T GRCh37
NC_000011.8:g.71469382G>T NCBI36
NG_021423.1:g.5353G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-337G>T (LRRC51) ENSP00000289488.2:n.-337G>T
ENST00000535883.6:c.-214G>T (LRRC51) ENSP00000437561.1:n.-214G>T
ENST00000538413.6:c.-253G>T (LRRC51) ENSP00000438762.2:n.-253G>T
ENST00000539271.6:c.-407G>T (LRRC51) ENSP00000442267.2:n.-407G>T
ENST00000642510.1:c.-530G>T (LRRC51) ENSP00000496544.1:n.-530G>T
ENST00000642648.1:c.-214G>T (LRRC51) ENSP00000494362.1:n.-214G>T
ENST00000642813.1:n.123G>T (LRRC51)
ENST00000647530.1:c.-500G>T (LRRC51) ENSP00000494072.1:n.-500G>T
ENST00000289488.6:c.-337G>T (LRRC51) ENSP00000289488.2:n.-337G>T
ENST00000307198.11:c.-519G>T (LRRC51) ENSP00000305742.7:n.-519G>T
ENST00000535883.5:c.-337G>T (LRRC51) ENSP00000437561.1:n.-337G>T
ENST00000538413.5:c.-214G>T (LRRC51) ENSP00000438762.1:n.-214G>T
ENST00000543450.1:n.6C>A (NUMA1)
ENST00000613205.4:c.-333C>A (NUMA1) ENSP00000480172.1:n.-333C>A
NM_001145307.4:c.-337G>T (LRTOMT) NP_001138779.1:n.-337G>T
NM_001145308.4:c.-519G>T (LRTOMT) NP_001138780.1:n.-519G>T
NM_001145309.3:c.-740G>T (LRTOMT) NP_001138781.1:n.-740G>T
NM_001145310.3:c.-740G>T (LRTOMT) NP_001138782.1:n.-740G>T
NM_001205138.3:c.-254G>T (LRTOMT) NP_001192067.1:n.-254G>T
NM_001271471.2:c.-337G>T (LRTOMT) NP_001258400.1:n.-337G>T
NM_001286561.1:c.-431C>A (NUMA1) NP_001273490.1:n.-431C>A
NM_006185.3:c.-333C>A (NUMA1) NP_006176.2:n.-333C>A
NM_145309.5:c.-337G>T (LRTOMT) NP_660352.1:n.-337G>T
NR_026886.3:n.358G>T (LRTOMT)
XM_006718473.2:c.-214G>T (LRTOMT) XP_006718536.1:n.-214G>T
NM_001318803.1:c.-294G>T (LRTOMT) NP_001305732.1:n.-294G>T
NR_134858.1:n.358G>T (LRTOMT)
XM_006718473.4:c.-214G>T (LRTOMT) XP_006718536.1:n.-214G>T
XM_006718474.4:c.-253G>T (LRTOMT) XP_006718537.1:n.-253G>T
XM_011544848.3:c.-500G>T (LRTOMT) XP_011543150.1:n.-500G>T