Canonical Allele Identifier: CA2614917041
Gene: LRTOMT HGNC NCBI
LRRC51 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72105801_72105802del , CM000673.2:g.72105801_72105802del GRCh38
NC_000011.9:g.71816847_71816848del , CM000673.1:g.71816847_71816848del GRCh37
NC_000011.8:g.71494495_71494496del NCBI36
NG_021423.1:g.30466_30467del

Transcript Alleles

HGVS Amino-acid Change
ENST00000643715.1:c.438-2804_438-2803del (LRTOMT) ENSP00000496019.1:n.438-2804_438-2803del
ENST00000646163.1:c.73-255_73-254del (LRTOMT) ENSP00000494749.1:n.73-255_73-254del
ENST00000307198.11:c.84-135_84-134del (LRRC51) ENSP00000305742.7:n.84-135_84-134del
ENST00000419228.2:c.84-255_84-254del (LRRC51) ENSP00000392233.2:n.84-255_84-254del
ENST00000427369.6:c.487-135_487-134del (LRRC51) ENSP00000409403.2:n.487-135_487-134del
ENST00000435085.5:c.84-135_84-134del (LRRC51) ENSP00000409789.1:n.84-135_84-134del
ENST00000439209.5:c.438-2804_438-2803del (LRRC51) ENSP00000395139.1:n.438-2804_438-2803del
ENST00000541899.1:n.7_8del (LRRC51)
ENST00000544409.5:c.487-255_487-254del (LRRC51) ENSP00000440969.1:n.487-255_487-254del
NM_001145308.4:c.84-135_84-134del (LRTOMT) NP_001138780.1:n.84-135_84-134del
NM_001145309.3:c.84-135_84-134del (LRTOMT) NP_001138781.1:n.84-135_84-134del
NM_001145310.3:c.84-255_84-254del (LRTOMT) NP_001138782.1:n.84-255_84-254del
XM_011544849.1:c.309-135_309-134del (LRTOMT) XP_011543151.1:n.309-135_309-134del
XM_024448401.1:c.309-135_309-134del (LRTOMT) XP_024304169.1:n.309-135_309-134del
NM_001145308.5:c.84-135_84-134del (LRTOMT) NP_001138780.1:n.84-135_84-134del
NM_001145309.4:c.84-135_84-134del (LRTOMT) NP_001138781.1:n.84-135_84-134del
NM_001145310.4:c.84-255_84-254del (LRTOMT) NP_001138782.1:n.84-255_84-254del