Canonical Allele Identifier: CA2790314376
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617831_6617832insAGT , CM000673.2:g.6617831_6617832insAGT GRCh38
NC_000011.9:g.6639062_6639063insAGT , CM000673.1:g.6639062_6639063insAGT GRCh37
NC_000011.8:g.6595638_6595639insAGT NCBI36
NG_008653.1:g.6630_6631insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-56_116-55insACT ENSP00000507321.1:n.116-56_116-55insACT
ENST00000299427.12:c.230-56_230-55insACT MANE Select ENSP00000299427.6:n.230-56_230-55insACT
ENST00000428886.7:n.318-56_318-55insACT
ENST00000436873.7:c.34-56_34-55insACT
ENST00000524788.2:n.1186_1187insACT
ENST00000524903.2:n.1302_1303insACT
ENST00000528571.6:c.90-56_90-55insACT ENSP00000434647.1:n.90-56_90-55insACT
ENST00000530040.2:n.259-56_259-55insACT
ENST00000533371.6:c.-500-56_-500-55insACT ENSP00000437066.1:n.-500-56_-500-55insACT
ENST00000534644.6:n.231-56_231-55insACT
ENST00000642892.1:c.-447-56_-447-55insACT ENSP00000494165.1:n.-447-56_-447-55insACT
ENST00000643439.1:c.90-56_90-55insACT ENSP00000495849.1:n.90-56_90-55insACT
ENST00000643479.1:n.259-56_259-55insACT
ENST00000643516.1:c.117-56_117-55insACT
ENST00000644151.1:n.1466_1467insACT
ENST00000644218.1:c.230-56_230-55insACT ENSP00000493574.1:n.230-56_230-55insACT
ENST00000644683.1:c.230-56_230-55insACT ENSP00000494085.1:n.230-56_230-55insACT
ENST00000644810.1:c.230-679_230-678insACT ENSP00000495895.1:n.230-679_230-678insACT
ENST00000644831.1:n.259-56_259-55insACT
ENST00000644933.1:c.-500-56_-500-55insACT ENSP00000496133.1:n.-500-56_-500-55insACT
ENST00000645020.1:n.1202_1203insACT
ENST00000645285.1:c.-500-56_-500-55insACT ENSP00000495058.1:n.-500-56_-500-55insACT
ENST00000645331.1:n.252-56_252-55insACT
ENST00000645620.1:c.-442-56_-442-55insACT ENSP00000493657.1:n.-442-56_-442-55insACT
ENST00000646777.1:n.259-56_259-55insACT
ENST00000647016.1:n.507_508insACT
ENST00000647152.1:c.-500-56_-500-55insACT ENSP00000495893.1:n.-500-56_-500-55insACT
ENST00000647209.1:c.*99-56_*99-55insACT ENSP00000495558.1:n.*99-56_*99-55insACT
ENST00000647346.1:n.1194_1195insACT
ENST00000299427.10:c.230-56_230-55insACT ENSP00000299427.6:n.230-56_230-55insACT
ENST00000428886.6:n.252-56_252-55insACT
ENST00000436873.6:c.230-56_230-55insACT ENSP00000398136.2:n.230-56_230-55insACT
ENST00000528571.5:c.90-56_90-55insACT ENSP00000434647.1:n.90-56_90-55insACT
ENST00000528917.1:n.531-56_531-55insACT
ENST00000530040.1:n.342-56_342-55insACT
ENST00000533371.5:c.-500-56_-500-55insACT ENSP00000437066.1:n.-500-56_-500-55insACT
ENST00000534644.5:n.215-56_215-55insACT
ENST00000611494.4:c.230-56_230-55insACT ENSP00000484546.1:n.230-56_230-55insACT
NM_000391.3:c.230-56_230-55insACT NP_000382.3:n.230-56_230-55insACT
NM_000391.4:c.230-56_230-55insACT MANE Select NP_000382.3:n.230-56_230-55insACT