Canonical Allele Identifier: CA2790314377
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617834_6617838del , CM000673.2:g.6617834_6617838del GRCh38
NC_000011.9:g.6639065_6639069del , CM000673.1:g.6639065_6639069del GRCh37
NC_000011.8:g.6595641_6595645del NCBI36
NG_008653.1:g.6624_6628del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-62_116-58del ENSP00000507321.1:n.116-62_116-58del
ENST00000299427.12:c.230-62_230-58del MANE Select ENSP00000299427.6:n.230-62_230-58del
ENST00000428886.7:n.318-62_318-58del
ENST00000436873.7:c.34-62_34-58del
ENST00000524788.2:n.1180_1184del
ENST00000524903.2:n.1296_1300del
ENST00000528571.6:c.90-62_90-58del ENSP00000434647.1:n.90-62_90-58del
ENST00000530040.2:n.259-62_259-58del
ENST00000533371.6:c.-500-62_-500-58del ENSP00000437066.1:n.-500-62_-500-58del
ENST00000534644.6:n.231-62_231-58del
ENST00000642892.1:c.-447-62_-447-58del ENSP00000494165.1:n.-447-62_-447-58del
ENST00000643439.1:c.90-62_90-58del ENSP00000495849.1:n.90-62_90-58del
ENST00000643479.1:n.259-62_259-58del
ENST00000643516.1:c.117-62_117-58del
ENST00000644151.1:n.1460_1464del
ENST00000644218.1:c.230-62_230-58del ENSP00000493574.1:n.230-62_230-58del
ENST00000644683.1:c.230-62_230-58del ENSP00000494085.1:n.230-62_230-58del
ENST00000644810.1:c.230-685_230-681del ENSP00000495895.1:n.230-685_230-681del
ENST00000644831.1:n.259-62_259-58del
ENST00000644933.1:c.-500-62_-500-58del ENSP00000496133.1:n.-500-62_-500-58del
ENST00000645020.1:n.1196_1200del
ENST00000645285.1:c.-500-62_-500-58del ENSP00000495058.1:n.-500-62_-500-58del
ENST00000645331.1:n.252-62_252-58del
ENST00000645620.1:c.-442-62_-442-58del ENSP00000493657.1:n.-442-62_-442-58del
ENST00000646777.1:n.259-62_259-58del
ENST00000647016.1:n.501_505del
ENST00000647152.1:c.-500-62_-500-58del ENSP00000495893.1:n.-500-62_-500-58del
ENST00000647209.1:c.*99-62_*99-58del ENSP00000495558.1:n.*99-62_*99-58del
ENST00000647346.1:n.1188_1192del
ENST00000299427.10:c.230-62_230-58del ENSP00000299427.6:n.230-62_230-58del
ENST00000428886.6:n.252-62_252-58del
ENST00000436873.6:c.230-62_230-58del ENSP00000398136.2:n.230-62_230-58del
ENST00000528571.5:c.90-62_90-58del ENSP00000434647.1:n.90-62_90-58del
ENST00000528917.1:n.531-62_531-58del
ENST00000530040.1:n.342-62_342-58del
ENST00000533371.5:c.-500-62_-500-58del ENSP00000437066.1:n.-500-62_-500-58del
ENST00000534644.5:n.215-62_215-58del
ENST00000611494.4:c.230-62_230-58del ENSP00000484546.1:n.230-62_230-58del
NM_000391.3:c.230-62_230-58del NP_000382.3:n.230-62_230-58del
NM_000391.4:c.230-62_230-58del MANE Select NP_000382.3:n.230-62_230-58del