Canonical Allele Identifier: CA2614916579
Gene: LRRC51 HGNC NCBI
LRTOMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080729T>C , CM000673.2:g.72080729T>C GRCh38
NC_000011.9:g.71791775T>C , CM000673.1:g.71791775T>C GRCh37
NC_000011.8:g.71469423T>C NCBI36
NG_021423.1:g.5394T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-296T>C (LRRC51) ENSP00000289488.2:n.-296T>C
ENST00000535883.6:c.-173T>C (LRRC51) ENSP00000437561.1:n.-173T>C
ENST00000538413.6:c.-212T>C (LRRC51) ENSP00000438762.2:n.-212T>C
ENST00000539271.6:c.-366T>C (LRRC51) ENSP00000442267.2:n.-366T>C
ENST00000642510.1:c.-489T>C (LRRC51) ENSP00000496544.1:n.-489T>C
ENST00000642648.1:c.-173T>C (LRRC51) ENSP00000494362.1:n.-173T>C
ENST00000642813.1:n.164T>C (LRRC51)
ENST00000647530.1:c.-459T>C (LRRC51) ENSP00000494072.1:n.-459T>C
ENST00000289488.6:c.-296T>C (LRRC51) ENSP00000289488.2:n.-296T>C
ENST00000307198.11:c.-478T>C (LRRC51) ENSP00000305742.7:n.-478T>C
ENST00000535883.5:c.-296T>C (LRRC51) ENSP00000437561.1:n.-296T>C
ENST00000538413.5:c.-173T>C (LRRC51) ENSP00000438762.1:n.-173T>C
NM_001145307.4:c.-296T>C (LRTOMT) NP_001138779.1:n.-296T>C
NM_001145308.4:c.-478T>C (LRTOMT) NP_001138780.1:n.-478T>C
NM_001145309.3:c.-699T>C (LRTOMT) NP_001138781.1:n.-699T>C
NM_001145310.3:c.-699T>C (LRTOMT) NP_001138782.1:n.-699T>C
NM_001205138.3:c.-213T>C (LRTOMT) NP_001192067.1:n.-213T>C
NM_001271471.2:c.-296T>C (LRTOMT) NP_001258400.1:n.-296T>C
NM_145309.5:c.-296T>C (LRTOMT) NP_660352.1:n.-296T>C
NR_026886.3:n.399T>C (LRTOMT)
XM_006718473.2:c.-173T>C (LRTOMT) XP_006718536.1:n.-173T>C
NM_001318803.1:c.-253T>C (LRTOMT) NP_001305732.1:n.-253T>C
NR_134858.1:n.399T>C (LRTOMT)
XM_006718473.4:c.-173T>C (LRTOMT) XP_006718536.1:n.-173T>C
XM_006718474.4:c.-212T>C (LRTOMT) XP_006718537.1:n.-212T>C
XM_011544848.3:c.-459T>C (LRTOMT) XP_011543150.1:n.-459T>C