Canonical Allele Identifier: CA2614916625
Gene: LRRC51 HGNC NCBI
LRTOMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080744T>G , CM000673.2:g.72080744T>G GRCh38
NC_000011.9:g.71791790T>G , CM000673.1:g.71791790T>G GRCh37
NC_000011.8:g.71469438T>G NCBI36
NG_021423.1:g.5409T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-281T>G (LRRC51) ENSP00000289488.2:n.-281T>G
ENST00000535883.6:c.-158T>G (LRRC51) ENSP00000437561.1:n.-158T>G
ENST00000538413.6:c.-197T>G (LRRC51) ENSP00000438762.2:n.-197T>G
ENST00000539271.6:c.-351T>G (LRRC51) ENSP00000442267.2:n.-351T>G
ENST00000642510.1:c.-474T>G (LRRC51) ENSP00000496544.1:n.-474T>G
ENST00000642648.1:c.-158T>G (LRRC51) ENSP00000494362.1:n.-158T>G
ENST00000642813.1:n.179T>G (LRRC51)
ENST00000647530.1:c.-444T>G (LRRC51) ENSP00000494072.1:n.-444T>G
ENST00000289488.6:c.-281T>G (LRRC51) ENSP00000289488.2:n.-281T>G
ENST00000307198.11:c.-463T>G (LRRC51) ENSP00000305742.7:n.-463T>G
ENST00000535883.5:c.-281T>G (LRRC51) ENSP00000437561.1:n.-281T>G
ENST00000538413.5:c.-158T>G (LRRC51) ENSP00000438762.1:n.-158T>G
NM_001145307.4:c.-281T>G (LRTOMT) NP_001138779.1:n.-281T>G
NM_001145308.4:c.-463T>G (LRTOMT) NP_001138780.1:n.-463T>G
NM_001145309.3:c.-684T>G (LRTOMT) NP_001138781.1:n.-684T>G
NM_001145310.3:c.-684T>G (LRTOMT) NP_001138782.1:n.-684T>G
NM_001205138.3:c.-198T>G (LRTOMT) NP_001192067.1:n.-198T>G
NM_001271471.2:c.-281T>G (LRTOMT) NP_001258400.1:n.-281T>G
NM_145309.5:c.-281T>G (LRTOMT) NP_660352.1:n.-281T>G
NR_026886.3:n.414T>G (LRTOMT)
XM_006718473.2:c.-158T>G (LRTOMT) XP_006718536.1:n.-158T>G
NM_001318803.1:c.-238T>G (LRTOMT) NP_001305732.1:n.-238T>G
NR_134858.1:n.414T>G (LRTOMT)
XM_006718473.4:c.-158T>G (LRTOMT) XP_006718536.1:n.-158T>G
XM_006718474.4:c.-197T>G (LRTOMT) XP_006718537.1:n.-197T>G
XM_011544848.3:c.-444T>G (LRTOMT) XP_011543150.1:n.-444T>G