Canonical Allele Identifier: CA918911919
Gene: LRTOMT HGNC NCBI
LRRC51 HGNC NCBI

Linked Data

dbSNP Id: rs1565329565

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72105876del , CM000673.2:g.72105876del GRCh38
NC_000011.9:g.71816922del , CM000673.1:g.71816922del GRCh37
NC_000011.8:g.71494570del NCBI36
NG_021423.1:g.30541del

Transcript Alleles

HGVS Amino-acid Change
ENST00000643715.1:c.438-2729del (LRTOMT) ENSP00000496019.1:n.438-2729del
ENST00000646163.1:c.73-180del (LRTOMT) ENSP00000494749.1:n.73-180del
ENST00000307198.11:c.84-60del (LRRC51) ENSP00000305742.7:n.84-60del
ENST00000419228.2:c.84-180del (LRRC51) ENSP00000392233.2:n.84-180del
ENST00000427369.6:c.487-60del (LRRC51) ENSP00000409403.2:n.487-60del
ENST00000435085.5:c.84-60del (LRRC51) ENSP00000409789.1:n.84-60del
ENST00000439209.5:c.438-2729del (LRRC51) ENSP00000395139.1:n.438-2729del
ENST00000541899.1:n.82del (LRRC51)
ENST00000544409.5:c.487-180del (LRRC51) ENSP00000440969.1:n.487-180del
NM_001145308.4:c.84-60del (LRTOMT) NP_001138780.1:n.84-60del
NM_001145309.3:c.84-60del (LRTOMT) NP_001138781.1:n.84-60del
NM_001145310.3:c.84-180del (LRTOMT) NP_001138782.1:n.84-180del
XM_011544849.1:c.309-60del (LRTOMT) XP_011543151.1:n.309-60del
XM_024448401.1:c.309-60del (LRTOMT) XP_024304169.1:n.309-60del
NM_001145308.5:c.84-60del (LRTOMT) NP_001138780.1:n.84-60del
NM_001145309.4:c.84-60del (LRTOMT) NP_001138781.1:n.84-60del
NM_001145310.4:c.84-180del (LRTOMT) NP_001138782.1:n.84-180del