Canonical Allele Identifier: CA2614916557
Gene: LRRC51 HGNC NCBI
LRTOMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080723G>A , CM000673.2:g.72080723G>A GRCh38
NC_000011.9:g.71791769G>A , CM000673.1:g.71791769G>A GRCh37
NC_000011.8:g.71469417G>A NCBI36
NG_021423.1:g.5388G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-302G>A (LRRC51) ENSP00000289488.2:n.-302G>A
ENST00000535883.6:c.-179G>A (LRRC51) ENSP00000437561.1:n.-179G>A
ENST00000538413.6:c.-218G>A (LRRC51) ENSP00000438762.2:n.-218G>A
ENST00000539271.6:c.-372G>A (LRRC51) ENSP00000442267.2:n.-372G>A
ENST00000642510.1:c.-495G>A (LRRC51) ENSP00000496544.1:n.-495G>A
ENST00000642648.1:c.-179G>A (LRRC51) ENSP00000494362.1:n.-179G>A
ENST00000642813.1:n.158G>A (LRRC51)
ENST00000647530.1:c.-465G>A (LRRC51) ENSP00000494072.1:n.-465G>A
ENST00000289488.6:c.-302G>A (LRRC51) ENSP00000289488.2:n.-302G>A
ENST00000307198.11:c.-484G>A (LRRC51) ENSP00000305742.7:n.-484G>A
ENST00000535883.5:c.-302G>A (LRRC51) ENSP00000437561.1:n.-302G>A
ENST00000538413.5:c.-179G>A (LRRC51) ENSP00000438762.1:n.-179G>A
NM_001145307.4:c.-302G>A (LRTOMT) NP_001138779.1:n.-302G>A
NM_001145308.4:c.-484G>A (LRTOMT) NP_001138780.1:n.-484G>A
NM_001145309.3:c.-705G>A (LRTOMT) NP_001138781.1:n.-705G>A
NM_001145310.3:c.-705G>A (LRTOMT) NP_001138782.1:n.-705G>A
NM_001205138.3:c.-219G>A (LRTOMT) NP_001192067.1:n.-219G>A
NM_001271471.2:c.-302G>A (LRTOMT) NP_001258400.1:n.-302G>A
NM_145309.5:c.-302G>A (LRTOMT) NP_660352.1:n.-302G>A
NR_026886.3:n.393G>A (LRTOMT)
XM_006718473.2:c.-179G>A (LRTOMT) XP_006718536.1:n.-179G>A
NM_001318803.1:c.-259G>A (LRTOMT) NP_001305732.1:n.-259G>A
NR_134858.1:n.393G>A (LRTOMT)
XM_006718473.4:c.-179G>A (LRTOMT) XP_006718536.1:n.-179G>A
XM_006718474.4:c.-218G>A (LRTOMT) XP_006718537.1:n.-218G>A
XM_011544848.3:c.-465G>A (LRTOMT) XP_011543150.1:n.-465G>A