Canonical Allele Identifier: CA1981839838

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72105946_72105960delinsGGGACCATGTCCCCT , CM000673.2:g.72105946_72105960delinsGGGACCATGTCCCCT GRCh38
NC_000011.9:g.71816992_71817006delinsGGGACCATGTCCCCT , CM000673.1:g.71816992_71817006delinsGGGACCATGTCCCCT GRCh37
NC_000011.8:g.71494640_71494654delinsGGGACCATGTCCCCT NCBI36
NG_021423.1:g.30611_30625delinsGGGACCATGTCCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000541899.3:c.-6_9delinsGGGACCATGTCCCCT (TOMT)
ENST00000541899.2:c.-6_9delinsGGGACCATGTCCCCT (TOMT)
ENST00000643715.1:c.438-2659_438-2645delinsGGGACCATGTCCCCT (LRTOMT) ENSP00000496019.1:n.438-2659_438-2645delinsGGGACCATGTCCCCT
ENST00000646163.1:c.73-110_73-96delinsGGGACCATGTCCCCT (LRTOMT) ENSP00000494749.1:n.73-110_73-96delinsGGGACCATGTCCCCT
ENST00000307198.11:c.94_108delinsGGGACCATGTCCCCT (LRRC51) ENSP00000305742.7:p.Gly32=
ENST00000419228.2:c.84-110_84-96delinsGGGACCATGTCCCCT (LRRC51) ENSP00000392233.2:n.84-110_84-96delinsGGGACCATGTCCCCT
ENST00000427369.6:c.497_511delinsGGGACCATGTCCCCT (LRRC51) ENSP00000409403.2:p.Arg166=
ENST00000435085.5:c.94_108delinsGGGACCATGTCCCCT (LRRC51) ENSP00000409789.1:p.Gly32=
ENST00000439209.5:c.438-2659_438-2645delinsGGGACCATGTCCCCT (LRRC51) ENSP00000395139.1:n.438-2659_438-2645delinsGGGACCATGTCCCCT
ENST00000541899.1:n.152_166delinsGGGACCATGTCCCCT (LRRC51)
ENST00000544409.5:c.487-110_487-96delinsGGGACCATGTCCCCT (LRRC51) ENSP00000440969.1:n.487-110_487-96delinsGGGACCATGTCCCCT
NM_001145308.4:c.94_108delinsGGGACCATGTCCCCT (LRTOMT) NP_001138780.1:p.Gly32=
NM_001145309.3:c.94_108delinsGGGACCATGTCCCCT (LRTOMT) NP_001138781.1:p.Gly32=
NM_001145310.3:c.84-110_84-96delinsGGGACCATGTCCCCT (LRTOMT) NP_001138782.1:n.84-110_84-96delinsGGGACCATGTCCCCT
XM_011544849.1:c.319_333delinsGGGACCATGTCCCCT (LRTOMT) XP_011543151.1:p.Gly107=
XM_024448401.1:c.319_333delinsGGGACCATGTCCCCT (LRTOMT) XP_024304169.1:p.Gly107=
NM_001145308.5:c.94_108delinsGGGACCATGTCCCCT (LRTOMT) NP_001138780.1:p.Gly32=
NM_001145309.4:c.94_108delinsGGGACCATGTCCCCT (LRTOMT) NP_001138781.1:p.Gly32=
NM_001145310.4:c.84-110_84-96delinsGGGACCATGTCCCCT (LRTOMT) NP_001138782.1:n.84-110_84-96delinsGGGACCATGTCCCCT
NM_001393500.1:c.-6_9delinsGGGACCATGTCCCCT (TOMT)
NM_001393500.2:c.-6_9delinsGGGACCATGTCCCCT (TOMT)