Canonical Allele Identifier: CA1981828495
Gene: LRRC51 HGNC NCBI
LRTOMT HGNC NCBI

Linked Data

dbSNP Id: rs1944107128

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080755del , CM000673.2:g.72080755del GRCh38
NC_000011.9:g.71791801del , CM000673.1:g.71791801del GRCh37
NC_000011.8:g.71469449del NCBI36
NG_021423.1:g.5420del

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-270del (LRRC51) ENSP00000289488.2:n.-270del
ENST00000535883.6:c.-147del (LRRC51) ENSP00000437561.1:n.-147del
ENST00000538413.6:c.-186del (LRRC51) ENSP00000438762.2:n.-186del
ENST00000539271.6:c.-340del (LRRC51) ENSP00000442267.2:n.-340del
ENST00000642510.1:c.-463del (LRRC51) ENSP00000496544.1:n.-463del
ENST00000642648.1:c.-147del (LRRC51) ENSP00000494362.1:n.-147del
ENST00000642813.1:n.190del (LRRC51)
ENST00000647530.1:c.-433del (LRRC51) ENSP00000494072.1:n.-433del
ENST00000289488.6:c.-270del (LRRC51) ENSP00000289488.2:n.-270del
ENST00000307198.11:c.-452del (LRRC51) ENSP00000305742.7:n.-452del
ENST00000535883.5:c.-270del (LRRC51) ENSP00000437561.1:n.-270del
ENST00000538413.5:c.-147del (LRRC51) ENSP00000438762.1:n.-147del
NM_001145307.4:c.-270del (LRTOMT) NP_001138779.1:n.-270del
NM_001145308.4:c.-452del (LRTOMT) NP_001138780.1:n.-452del
NM_001145309.3:c.-673del (LRTOMT) NP_001138781.1:n.-673del
NM_001145310.3:c.-673del (LRTOMT) NP_001138782.1:n.-673del
NM_001205138.3:c.-187del (LRTOMT) NP_001192067.1:n.-187del
NM_001271471.2:c.-270del (LRTOMT) NP_001258400.1:n.-270del
NM_145309.5:c.-270del (LRTOMT) NP_660352.1:n.-270del
NR_026886.3:n.425del (LRTOMT)
XM_006718473.2:c.-147del (LRTOMT) XP_006718536.1:n.-147del
NM_001318803.1:c.-227del (LRTOMT) NP_001305732.1:n.-227del
NR_134858.1:n.425del (LRTOMT)
XM_006718473.4:c.-147del (LRTOMT) XP_006718536.1:n.-147del
XM_006718474.4:c.-186del (LRTOMT) XP_006718537.1:n.-186del
XM_011544848.3:c.-433del (LRTOMT) XP_011543150.1:n.-433del