Canonical Allele Identifier: CA2614917023
Gene: LRTOMT HGNC NCBI
LRRC51 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72105796_72105797insCTCC , CM000673.2:g.72105796_72105797insCTCC GRCh38
NC_000011.9:g.71816842_71816843insCTCC , CM000673.1:g.71816842_71816843insCTCC GRCh37
NC_000011.8:g.71494490_71494491insCTCC NCBI36
NG_021423.1:g.30461_30462insCTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000643715.1:c.438-2809_438-2808insCTCC (LRTOMT) ENSP00000496019.1:n.438-2809_438-2808insCTCC
ENST00000646163.1:c.73-260_73-259insCTCC (LRTOMT) ENSP00000494749.1:n.73-260_73-259insCTCC
ENST00000307198.11:c.84-140_84-139insCTCC (LRRC51) ENSP00000305742.7:n.84-140_84-139insCTCC
ENST00000419228.2:c.84-260_84-259insCTCC (LRRC51) ENSP00000392233.2:n.84-260_84-259insCTCC
ENST00000427369.6:c.487-140_487-139insCTCC (LRRC51) ENSP00000409403.2:n.487-140_487-139insCTCC
ENST00000435085.5:c.84-140_84-139insCTCC (LRRC51) ENSP00000409789.1:n.84-140_84-139insCTCC
ENST00000439209.5:c.438-2809_438-2808insCTCC (LRRC51) ENSP00000395139.1:n.438-2809_438-2808insCTCC
ENST00000541899.1:n.2_3insCTCC (LRRC51)
ENST00000544409.5:c.487-260_487-259insCTCC (LRRC51) ENSP00000440969.1:n.487-260_487-259insCTCC
NM_001145308.4:c.84-140_84-139insCTCC (LRTOMT) NP_001138780.1:n.84-140_84-139insCTCC
NM_001145309.3:c.84-140_84-139insCTCC (LRTOMT) NP_001138781.1:n.84-140_84-139insCTCC
NM_001145310.3:c.84-260_84-259insCTCC (LRTOMT) NP_001138782.1:n.84-260_84-259insCTCC
XM_011544849.1:c.309-140_309-139insCTCC (LRTOMT) XP_011543151.1:n.309-140_309-139insCTCC
XM_024448401.1:c.309-140_309-139insCTCC (LRTOMT) XP_024304169.1:n.309-140_309-139insCTCC
NM_001145308.5:c.84-140_84-139insCTCC (LRTOMT) NP_001138780.1:n.84-140_84-139insCTCC
NM_001145309.4:c.84-140_84-139insCTCC (LRTOMT) NP_001138781.1:n.84-140_84-139insCTCC
NM_001145310.4:c.84-260_84-259insCTCC (LRTOMT) NP_001138782.1:n.84-260_84-259insCTCC