Canonical Allele Identifier: CA2614916705
Gene: LRRC51 HGNC NCBI
LRTOMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080819G>T , CM000673.2:g.72080819G>T GRCh38
NC_000011.9:g.71791865G>T , CM000673.1:g.71791865G>T GRCh37
NC_000011.8:g.71469513G>T NCBI36
NG_021423.1:g.5484G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-206G>T (LRRC51) ENSP00000289488.2:n.-206G>T
ENST00000535883.6:c.-140+57G>T (LRRC51) ENSP00000437561.1:n.-140+57G>T
ENST00000538413.6:c.-122G>T (LRRC51) ENSP00000438762.2:n.-122G>T
ENST00000539271.6:c.-333+57G>T (LRRC51) ENSP00000442267.2:n.-333+57G>T
ENST00000642510.1:c.-399G>T (LRRC51) ENSP00000496544.1:n.-399G>T
ENST00000642648.1:c.-140+57G>T (LRRC51) ENSP00000494362.1:n.-140+57G>T
ENST00000642813.1:n.254G>T (LRRC51)
ENST00000646163.1:c.-399G>T (LRTOMT) ENSP00000494749.1:n.-399G>T
ENST00000647530.1:c.-369G>T (LRRC51) ENSP00000494072.1:n.-369G>T
ENST00000289488.6:c.-206G>T (LRRC51) ENSP00000289488.2:n.-206G>T
ENST00000307198.11:c.-388G>T (LRRC51) ENSP00000305742.7:n.-388G>T
ENST00000412777.6:n.43G>T (LRRC51)
ENST00000423494.6:c.-123G>T (LRRC51) ENSP00000441249.1:n.-123G>T
ENST00000535883.5:c.-206G>T (LRRC51) ENSP00000437561.1:n.-206G>T
ENST00000538413.5:c.-140+57G>T (LRRC51) ENSP00000438762.1:n.-140+57G>T
ENST00000539271.5:c.-388G>T (LRRC51) ENSP00000442267.1:n.-388G>T
NM_001145307.4:c.-206G>T (LRTOMT) NP_001138779.1:n.-206G>T
NM_001145308.4:c.-388G>T (LRTOMT) NP_001138780.1:n.-388G>T
NM_001145309.3:c.-609G>T (LRTOMT) NP_001138781.1:n.-609G>T
NM_001145310.3:c.-609G>T (LRTOMT) NP_001138782.1:n.-609G>T
NM_001205138.3:c.-123G>T (LRTOMT) NP_001192067.1:n.-123G>T
NM_001271471.2:c.-206G>T (LRTOMT) NP_001258400.1:n.-206G>T
NM_145309.5:c.-206G>T (LRTOMT) NP_660352.1:n.-206G>T
NR_026886.3:n.489G>T (LRTOMT)
XM_006718472.2:c.-163G>T (LRTOMT) XP_006718535.1:n.-163G>T
XM_006718473.2:c.-140+57G>T (LRTOMT) XP_006718536.1:n.-140+57G>T
XM_006718474.2:c.-122G>T (LRTOMT) XP_006718537.1:n.-122G>T
XM_011544847.1:c.-311G>T (LRTOMT) XP_011543149.1:n.-311G>T
XM_011544848.1:c.-369G>T (LRTOMT) XP_011543150.1:n.-369G>T
NM_001318803.1:c.-163G>T (LRTOMT) NP_001305732.1:n.-163G>T
NR_134858.1:n.489G>T (LRTOMT)
XM_006718473.4:c.-140+57G>T (LRTOMT) XP_006718536.1:n.-140+57G>T
XM_006718474.4:c.-122G>T (LRTOMT) XP_006718537.1:n.-122G>T
XM_011544847.3:c.-311G>T (LRTOMT) XP_011543149.1:n.-311G>T
XM_011544848.3:c.-369G>T (LRTOMT) XP_011543150.1:n.-369G>T