Canonical Allele Identifier: CA2614916559
Gene: LRRC51 HGNC NCBI
LRTOMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080724C>T , CM000673.2:g.72080724C>T GRCh38
NC_000011.9:g.71791770C>T , CM000673.1:g.71791770C>T GRCh37
NC_000011.8:g.71469418C>T NCBI36
NG_021423.1:g.5389C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-301C>T (LRRC51) ENSP00000289488.2:n.-301C>T
ENST00000535883.6:c.-178C>T (LRRC51) ENSP00000437561.1:n.-178C>T
ENST00000538413.6:c.-217C>T (LRRC51) ENSP00000438762.2:n.-217C>T
ENST00000539271.6:c.-371C>T (LRRC51) ENSP00000442267.2:n.-371C>T
ENST00000642510.1:c.-494C>T (LRRC51) ENSP00000496544.1:n.-494C>T
ENST00000642648.1:c.-178C>T (LRRC51) ENSP00000494362.1:n.-178C>T
ENST00000642813.1:n.159C>T (LRRC51)
ENST00000647530.1:c.-464C>T (LRRC51) ENSP00000494072.1:n.-464C>T
ENST00000289488.6:c.-301C>T (LRRC51) ENSP00000289488.2:n.-301C>T
ENST00000307198.11:c.-483C>T (LRRC51) ENSP00000305742.7:n.-483C>T
ENST00000535883.5:c.-301C>T (LRRC51) ENSP00000437561.1:n.-301C>T
ENST00000538413.5:c.-178C>T (LRRC51) ENSP00000438762.1:n.-178C>T
NM_001145307.4:c.-301C>T (LRTOMT) NP_001138779.1:n.-301C>T
NM_001145308.4:c.-483C>T (LRTOMT) NP_001138780.1:n.-483C>T
NM_001145309.3:c.-704C>T (LRTOMT) NP_001138781.1:n.-704C>T
NM_001145310.3:c.-704C>T (LRTOMT) NP_001138782.1:n.-704C>T
NM_001205138.3:c.-218C>T (LRTOMT) NP_001192067.1:n.-218C>T
NM_001271471.2:c.-301C>T (LRTOMT) NP_001258400.1:n.-301C>T
NM_145309.5:c.-301C>T (LRTOMT) NP_660352.1:n.-301C>T
NR_026886.3:n.394C>T (LRTOMT)
XM_006718473.2:c.-178C>T (LRTOMT) XP_006718536.1:n.-178C>T
NM_001318803.1:c.-258C>T (LRTOMT) NP_001305732.1:n.-258C>T
NR_134858.1:n.394C>T (LRTOMT)
XM_006718473.4:c.-178C>T (LRTOMT) XP_006718536.1:n.-178C>T
XM_006718474.4:c.-217C>T (LRTOMT) XP_006718537.1:n.-217C>T
XM_011544848.3:c.-464C>T (LRTOMT) XP_011543150.1:n.-464C>T