Canonical Allele Identifier: CA1981841012

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72108601_72108602delinsAC , CM000673.2:g.72108601_72108602delinsAC GRCh38
NC_000011.9:g.71819647_71819648delinsAC , CM000673.1:g.71819647_71819648delinsAC GRCh37
NC_000011.8:g.71497295_71497296delinsAC NCBI36
NG_021423.1:g.33266_33267delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000541899.3:c.457-4_457-3delinsAC (TOMT) MANE Select ENSP00000494667.1:n.457-4_457-3delinsAC
ENST00000541899.2:c.457-4_457-3delinsAC (TOMT) ENSP00000494667.1:n.457-4_457-3delinsAC
ENST00000643715.1:c.438-4_438-3delinsAC (LRTOMT) ENSP00000496019.1:n.438-4_438-3delinsAC
ENST00000307198.11:c.556-4_556-3delinsAC (LRRC51) ENSP00000305742.7:n.556-4_556-3delinsAC
ENST00000419228.2:c.435-4_435-3delinsAC (LRRC51) ENSP00000392233.2:n.435-4_435-3delinsAC
ENST00000427369.6:c.*275-4_*275-3delinsAC (LRRC51) ENSP00000409403.2:n.*275-4_*275-3delinsAC
ENST00000435085.5:c.556-4_556-3delinsAC (LRRC51) ENSP00000409789.1:n.556-4_556-3delinsAC
ENST00000439209.5:c.438-4_438-3delinsAC (LRRC51) ENSP00000395139.1:n.438-4_438-3delinsAC
ENST00000502597.2:c.64-997_64-996delinsGT (ANAPC15) ENSP00000441774.1:n.64-997_64-996delinsGT
ENST00000543050.5:c.319-997_319-996delinsGT (ANAPC15) ENSP00000437360.1:n.319-997_319-996delinsGT
ENST00000544409.5:c.*275-4_*275-3delinsAC (LRRC51) ENSP00000440969.1:n.*275-4_*275-3delinsAC
NM_001145308.4:c.556-4_556-3delinsAC (LRTOMT) NP_001138780.1:n.556-4_556-3delinsAC
NM_001145309.3:c.556-4_556-3delinsAC (LRTOMT) NP_001138781.1:n.556-4_556-3delinsAC
NM_001145310.3:c.436-4_436-3delinsAC (LRTOMT) NP_001138782.1:n.436-4_436-3delinsAC
XM_011544849.1:c.781-4_781-3delinsAC (LRTOMT) XP_011543151.1:n.781-4_781-3delinsAC
NM_001330321.1:c.319-997_319-996delinsGT (ANAPC15) NP_001317250.1:n.319-997_319-996delinsGT
XM_024448401.1:c.781-4_781-3delinsAC (LRTOMT) XP_024304169.1:n.781-4_781-3delinsAC
NM_001145308.5:c.556-4_556-3delinsAC (LRTOMT) NP_001138780.1:n.556-4_556-3delinsAC
NM_001145309.4:c.556-4_556-3delinsAC (LRTOMT) NP_001138781.1:n.556-4_556-3delinsAC
NM_001145310.4:c.436-4_436-3delinsAC (LRTOMT) NP_001138782.1:n.436-4_436-3delinsAC
NM_001330321.2:c.319-997_319-996delinsGT (ANAPC15) NP_001317250.1:n.319-997_319-996delinsGT
NM_001393427.1:c.319-997_319-996delinsGT (ANAPC15) NP_001380356.1:n.319-997_319-996delinsGT
NM_001393428.1:c.319-997_319-996delinsGT (ANAPC15) NP_001380357.1:n.319-997_319-996delinsGT
NM_001393429.1:c.319-997_319-996delinsGT (ANAPC15) NP_001380358.1:n.319-997_319-996delinsGT
NM_001393430.1:c.319-997_319-996delinsGT (ANAPC15) NP_001380359.1:n.319-997_319-996delinsGT
NM_001393431.1:c.319-997_319-996delinsGT (ANAPC15) NP_001380360.1:n.319-997_319-996delinsGT
NM_001393443.1:c.*217_*218delinsGT (ANAPC15) NP_001380372.1:n.*217_*218delinsGT
NM_001393444.1:c.*217_*218delinsGT (ANAPC15) NP_001380373.1:n.*217_*218delinsGT
NM_001393445.1:c.*217_*218delinsGT (ANAPC15) NP_001380374.1:n.*217_*218delinsGT
NM_001393459.1:c.64-997_64-996delinsGT (ANAPC15) NP_001380388.1:n.64-997_64-996delinsGT
NM_001393500.1:c.457-4_457-3delinsAC (TOMT) NP_001380429.1:n.457-4_457-3delinsAC
NR_171687.1:n.841_842delinsGT (ANAPC15)
NM_001393500.2:c.457-4_457-3delinsAC (TOMT) MANE Select NP_001380429.1:n.457-4_457-3delinsAC