Canonical Allele Identifier: CA2790314450
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617945_6617949del , CM000673.2:g.6617945_6617949del GRCh38
NC_000011.9:g.6639176_6639180del , CM000673.1:g.6639176_6639180del GRCh37
NC_000011.8:g.6595752_6595756del NCBI36
NG_008653.1:g.6514_6518del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-172_116-168del ENSP00000507321.1:n.116-172_116-168del
ENST00000299427.12:c.230-172_230-168del MANE Select ENSP00000299427.6:n.230-172_230-168del
ENST00000428886.7:n.318-172_318-168del
ENST00000436873.7:c.34-172_34-168del
ENST00000524788.2:n.1070_1074del
ENST00000524903.2:n.1186_1190del
ENST00000528571.6:c.90-172_90-168del ENSP00000434647.1:n.90-172_90-168del
ENST00000530040.2:n.259-172_259-168del
ENST00000533371.6:c.-500-172_-500-168del ENSP00000437066.1:n.-500-172_-500-168del
ENST00000534644.6:n.231-172_231-168del
ENST00000642892.1:c.-447-172_-447-168del ENSP00000494165.1:n.-447-172_-447-168del
ENST00000643439.1:c.90-172_90-168del ENSP00000495849.1:n.90-172_90-168del
ENST00000643479.1:n.259-172_259-168del
ENST00000643516.1:c.117-172_117-168del
ENST00000644151.1:n.1350_1354del
ENST00000644218.1:c.230-172_230-168del ENSP00000493574.1:n.230-172_230-168del
ENST00000644683.1:c.230-172_230-168del ENSP00000494085.1:n.230-172_230-168del
ENST00000644810.1:c.230-795_230-791del ENSP00000495895.1:n.230-795_230-791del
ENST00000644831.1:n.259-172_259-168del
ENST00000644933.1:c.-500-172_-500-168del ENSP00000496133.1:n.-500-172_-500-168del
ENST00000645020.1:n.1086_1090del
ENST00000645285.1:c.-500-172_-500-168del ENSP00000495058.1:n.-500-172_-500-168del
ENST00000645331.1:n.252-172_252-168del
ENST00000645620.1:c.-442-172_-442-168del ENSP00000493657.1:n.-442-172_-442-168del
ENST00000646777.1:n.259-172_259-168del
ENST00000647016.1:n.391_395del
ENST00000647152.1:c.-500-172_-500-168del ENSP00000495893.1:n.-500-172_-500-168del
ENST00000647209.1:c.*99-172_*99-168del ENSP00000495558.1:n.*99-172_*99-168del
ENST00000647346.1:n.1078_1082del
ENST00000299427.10:c.230-172_230-168del ENSP00000299427.6:n.230-172_230-168del
ENST00000428886.6:n.252-172_252-168del
ENST00000436873.6:c.230-172_230-168del ENSP00000398136.2:n.230-172_230-168del
ENST00000528571.5:c.90-172_90-168del ENSP00000434647.1:n.90-172_90-168del
ENST00000528917.1:n.531-172_531-168del
ENST00000530040.1:n.342-172_342-168del
ENST00000533371.5:c.-500-172_-500-168del ENSP00000437066.1:n.-500-172_-500-168del
ENST00000534644.5:n.215-172_215-168del
ENST00000611494.4:c.230-172_230-168del ENSP00000484546.1:n.230-172_230-168del
NM_000391.3:c.230-172_230-168del NP_000382.3:n.230-172_230-168del
NM_000391.4:c.230-172_230-168del MANE Select NP_000382.3:n.230-172_230-168del