Canonical Allele Identifier: CA2790314420
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617915_6617916del , CM000673.2:g.6617915_6617916del GRCh38
NC_000011.9:g.6639146_6639147del , CM000673.1:g.6639146_6639147del GRCh37
NC_000011.8:g.6595722_6595723del NCBI36
NG_008653.1:g.6548_6549del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-138_116-137del ENSP00000507321.1:n.116-138_116-137del
ENST00000299427.12:c.230-138_230-137del MANE Select ENSP00000299427.6:n.230-138_230-137del
ENST00000428886.7:n.318-138_318-137del
ENST00000436873.7:c.34-138_34-137del
ENST00000524788.2:n.1104_1105del
ENST00000524903.2:n.1220_1221del
ENST00000528571.6:c.90-138_90-137del ENSP00000434647.1:n.90-138_90-137del
ENST00000530040.2:n.259-138_259-137del
ENST00000533371.6:c.-500-138_-500-137del ENSP00000437066.1:n.-500-138_-500-137del
ENST00000534644.6:n.231-138_231-137del
ENST00000642892.1:c.-447-138_-447-137del ENSP00000494165.1:n.-447-138_-447-137del
ENST00000643439.1:c.90-138_90-137del ENSP00000495849.1:n.90-138_90-137del
ENST00000643479.1:n.259-138_259-137del
ENST00000643516.1:c.117-138_117-137del
ENST00000644151.1:n.1384_1385del
ENST00000644218.1:c.230-138_230-137del ENSP00000493574.1:n.230-138_230-137del
ENST00000644683.1:c.230-138_230-137del ENSP00000494085.1:n.230-138_230-137del
ENST00000644810.1:c.230-761_230-760del ENSP00000495895.1:n.230-761_230-760del
ENST00000644831.1:n.259-138_259-137del
ENST00000644933.1:c.-500-138_-500-137del ENSP00000496133.1:n.-500-138_-500-137del
ENST00000645020.1:n.1120_1121del
ENST00000645285.1:c.-500-138_-500-137del ENSP00000495058.1:n.-500-138_-500-137del
ENST00000645331.1:n.252-138_252-137del
ENST00000645620.1:c.-442-138_-442-137del ENSP00000493657.1:n.-442-138_-442-137del
ENST00000646777.1:n.259-138_259-137del
ENST00000647016.1:n.425_426del
ENST00000647152.1:c.-500-138_-500-137del ENSP00000495893.1:n.-500-138_-500-137del
ENST00000647209.1:c.*99-138_*99-137del ENSP00000495558.1:n.*99-138_*99-137del
ENST00000647346.1:n.1112_1113del
ENST00000299427.10:c.230-138_230-137del ENSP00000299427.6:n.230-138_230-137del
ENST00000428886.6:n.252-138_252-137del
ENST00000436873.6:c.230-138_230-137del ENSP00000398136.2:n.230-138_230-137del
ENST00000528571.5:c.90-138_90-137del ENSP00000434647.1:n.90-138_90-137del
ENST00000528917.1:n.531-138_531-137del
ENST00000530040.1:n.342-138_342-137del
ENST00000533371.5:c.-500-138_-500-137del ENSP00000437066.1:n.-500-138_-500-137del
ENST00000534644.5:n.215-138_215-137del
ENST00000611494.4:c.230-138_230-137del ENSP00000484546.1:n.230-138_230-137del
NM_000391.3:c.230-138_230-137del NP_000382.3:n.230-138_230-137del
NM_000391.4:c.230-138_230-137del MANE Select NP_000382.3:n.230-138_230-137del