Canonical Allele Identifier: CA939427168
Gene: LRRC51 HGNC NCBI
LRTOMT HGNC NCBI

Linked Data

dbSNP Id: rs1944103546

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080697del , CM000673.2:g.72080697del GRCh38
NC_000011.9:g.71791743del , CM000673.1:g.71791743del GRCh37
NC_000011.8:g.71469391del NCBI36
NG_021423.1:g.5362del

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-328del (LRRC51) ENSP00000289488.2:n.-328del
ENST00000535883.6:c.-205del (LRRC51) ENSP00000437561.1:n.-205del
ENST00000538413.6:c.-244del (LRRC51) ENSP00000438762.2:n.-244del
ENST00000539271.6:c.-398del (LRRC51) ENSP00000442267.2:n.-398del
ENST00000642510.1:c.-521del (LRRC51) ENSP00000496544.1:n.-521del
ENST00000642648.1:c.-205del (LRRC51) ENSP00000494362.1:n.-205del
ENST00000642813.1:n.132del (LRRC51)
ENST00000647530.1:c.-491del (LRRC51) ENSP00000494072.1:n.-491del
ENST00000289488.6:c.-328del (LRRC51) ENSP00000289488.2:n.-328del
ENST00000307198.11:c.-510del (LRRC51) ENSP00000305742.7:n.-510del
ENST00000535883.5:c.-328del (LRRC51) ENSP00000437561.1:n.-328del
ENST00000538413.5:c.-205del (LRRC51) ENSP00000438762.1:n.-205del
NM_001145307.4:c.-328del (LRTOMT) NP_001138779.1:n.-328del
NM_001145308.4:c.-510del (LRTOMT) NP_001138780.1:n.-510del
NM_001145309.3:c.-731del (LRTOMT) NP_001138781.1:n.-731del
NM_001145310.3:c.-731del (LRTOMT) NP_001138782.1:n.-731del
NM_001205138.3:c.-245del (LRTOMT) NP_001192067.1:n.-245del
NM_001271471.2:c.-328del (LRTOMT) NP_001258400.1:n.-328del
NM_145309.5:c.-328del (LRTOMT) NP_660352.1:n.-328del
NR_026886.3:n.367del (LRTOMT)
XM_006718473.2:c.-205del (LRTOMT) XP_006718536.1:n.-205del
NM_001318803.1:c.-285del (LRTOMT) NP_001305732.1:n.-285del
NR_134858.1:n.367del (LRTOMT)
XM_006718473.4:c.-205del (LRTOMT) XP_006718536.1:n.-205del
XM_006718474.4:c.-244del (LRTOMT) XP_006718537.1:n.-244del
XM_011544848.3:c.-491del (LRTOMT) XP_011543150.1:n.-491del