Canonical Allele Identifier: CA2790314429
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617918_6617924del , CM000673.2:g.6617918_6617924del GRCh38
NC_000011.9:g.6639149_6639155del , CM000673.1:g.6639149_6639155del GRCh37
NC_000011.8:g.6595725_6595731del NCBI36
NG_008653.1:g.6539_6545del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-147_116-141del ENSP00000507321.1:n.116-147_116-141del
ENST00000299427.12:c.230-147_230-141del MANE Select ENSP00000299427.6:n.230-147_230-141del
ENST00000428886.7:n.318-147_318-141del
ENST00000436873.7:c.34-147_34-141del
ENST00000524788.2:n.1095_1101del
ENST00000524903.2:n.1211_1217del
ENST00000528571.6:c.90-147_90-141del ENSP00000434647.1:n.90-147_90-141del
ENST00000530040.2:n.259-147_259-141del
ENST00000533371.6:c.-500-147_-500-141del ENSP00000437066.1:n.-500-147_-500-141del
ENST00000534644.6:n.231-147_231-141del
ENST00000642892.1:c.-447-147_-447-141del ENSP00000494165.1:n.-447-147_-447-141del
ENST00000643439.1:c.90-147_90-141del ENSP00000495849.1:n.90-147_90-141del
ENST00000643479.1:n.259-147_259-141del
ENST00000643516.1:c.117-147_117-141del
ENST00000644151.1:n.1375_1381del
ENST00000644218.1:c.230-147_230-141del ENSP00000493574.1:n.230-147_230-141del
ENST00000644683.1:c.230-147_230-141del ENSP00000494085.1:n.230-147_230-141del
ENST00000644810.1:c.230-770_230-764del ENSP00000495895.1:n.230-770_230-764del
ENST00000644831.1:n.259-147_259-141del
ENST00000644933.1:c.-500-147_-500-141del ENSP00000496133.1:n.-500-147_-500-141del
ENST00000645020.1:n.1111_1117del
ENST00000645285.1:c.-500-147_-500-141del ENSP00000495058.1:n.-500-147_-500-141del
ENST00000645331.1:n.252-147_252-141del
ENST00000645620.1:c.-442-147_-442-141del ENSP00000493657.1:n.-442-147_-442-141del
ENST00000646777.1:n.259-147_259-141del
ENST00000647016.1:n.416_422del
ENST00000647152.1:c.-500-147_-500-141del ENSP00000495893.1:n.-500-147_-500-141del
ENST00000647209.1:c.*99-147_*99-141del ENSP00000495558.1:n.*99-147_*99-141del
ENST00000647346.1:n.1103_1109del
ENST00000299427.10:c.230-147_230-141del ENSP00000299427.6:n.230-147_230-141del
ENST00000428886.6:n.252-147_252-141del
ENST00000436873.6:c.230-147_230-141del ENSP00000398136.2:n.230-147_230-141del
ENST00000528571.5:c.90-147_90-141del ENSP00000434647.1:n.90-147_90-141del
ENST00000528917.1:n.531-147_531-141del
ENST00000530040.1:n.342-147_342-141del
ENST00000533371.5:c.-500-147_-500-141del ENSP00000437066.1:n.-500-147_-500-141del
ENST00000534644.5:n.215-147_215-141del
ENST00000611494.4:c.230-147_230-141del ENSP00000484546.1:n.230-147_230-141del
NM_000391.3:c.230-147_230-141del NP_000382.3:n.230-147_230-141del
NM_000391.4:c.230-147_230-141del MANE Select NP_000382.3:n.230-147_230-141del