Canonical Allele Identifier: CA2790314440
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617929_6617947del , CM000673.2:g.6617929_6617947del GRCh38
NC_000011.9:g.6639160_6639178del , CM000673.1:g.6639160_6639178del GRCh37
NC_000011.8:g.6595736_6595754del NCBI36
NG_008653.1:g.6515_6533del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-171_116-153del ENSP00000507321.1:n.116-171_116-153del
ENST00000299427.12:c.230-171_230-153del MANE Select ENSP00000299427.6:n.230-171_230-153del
ENST00000428886.7:n.318-171_318-153del
ENST00000436873.7:c.34-171_34-153del
ENST00000524788.2:n.1071_1089del
ENST00000524903.2:n.1187_1205del
ENST00000528571.6:c.90-171_90-153del ENSP00000434647.1:n.90-171_90-153del
ENST00000530040.2:n.259-171_259-153del
ENST00000533371.6:c.-500-171_-500-153del ENSP00000437066.1:n.-500-171_-500-153del
ENST00000534644.6:n.231-171_231-153del
ENST00000642892.1:c.-447-171_-447-153del ENSP00000494165.1:n.-447-171_-447-153del
ENST00000643439.1:c.90-171_90-153del ENSP00000495849.1:n.90-171_90-153del
ENST00000643479.1:n.259-171_259-153del
ENST00000643516.1:c.117-171_117-153del
ENST00000644151.1:n.1351_1369del
ENST00000644218.1:c.230-171_230-153del ENSP00000493574.1:n.230-171_230-153del
ENST00000644683.1:c.230-171_230-153del ENSP00000494085.1:n.230-171_230-153del
ENST00000644810.1:c.230-794_230-776del ENSP00000495895.1:n.230-794_230-776del
ENST00000644831.1:n.259-171_259-153del
ENST00000644933.1:c.-500-171_-500-153del ENSP00000496133.1:n.-500-171_-500-153del
ENST00000645020.1:n.1087_1105del
ENST00000645285.1:c.-500-171_-500-153del ENSP00000495058.1:n.-500-171_-500-153del
ENST00000645331.1:n.252-171_252-153del
ENST00000645620.1:c.-442-171_-442-153del ENSP00000493657.1:n.-442-171_-442-153del
ENST00000646777.1:n.259-171_259-153del
ENST00000647016.1:n.392_410del
ENST00000647152.1:c.-500-171_-500-153del ENSP00000495893.1:n.-500-171_-500-153del
ENST00000647209.1:c.*99-171_*99-153del ENSP00000495558.1:n.*99-171_*99-153del
ENST00000647346.1:n.1079_1097del
ENST00000299427.10:c.230-171_230-153del ENSP00000299427.6:n.230-171_230-153del
ENST00000428886.6:n.252-171_252-153del
ENST00000436873.6:c.230-171_230-153del ENSP00000398136.2:n.230-171_230-153del
ENST00000528571.5:c.90-171_90-153del ENSP00000434647.1:n.90-171_90-153del
ENST00000528917.1:n.531-171_531-153del
ENST00000530040.1:n.342-171_342-153del
ENST00000533371.5:c.-500-171_-500-153del ENSP00000437066.1:n.-500-171_-500-153del
ENST00000534644.5:n.215-171_215-153del
ENST00000611494.4:c.230-171_230-153del ENSP00000484546.1:n.230-171_230-153del
NM_000391.3:c.230-171_230-153del NP_000382.3:n.230-171_230-153del
NM_000391.4:c.230-171_230-153del MANE Select NP_000382.3:n.230-171_230-153del