Canonical Allele Identifier: CA2790314457
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617953_6617954del , CM000673.2:g.6617953_6617954del GRCh38
NC_000011.9:g.6639184_6639185del , CM000673.1:g.6639184_6639185del GRCh37
NC_000011.8:g.6595760_6595761del NCBI36
NG_008653.1:g.6508_6509del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-178_116-177del ENSP00000507321.1:n.116-178_116-177del
ENST00000299427.12:c.230-178_230-177del MANE Select ENSP00000299427.6:n.230-178_230-177del
ENST00000428886.7:n.318-178_318-177del
ENST00000436873.7:c.34-178_34-177del
ENST00000524788.2:n.1064_1065del
ENST00000524903.2:n.1180_1181del
ENST00000528571.6:c.90-178_90-177del ENSP00000434647.1:n.90-178_90-177del
ENST00000530040.2:n.259-178_259-177del
ENST00000533371.6:c.-500-178_-500-177del ENSP00000437066.1:n.-500-178_-500-177del
ENST00000534644.6:n.231-178_231-177del
ENST00000642892.1:c.-447-178_-447-177del ENSP00000494165.1:n.-447-178_-447-177del
ENST00000643439.1:c.90-178_90-177del ENSP00000495849.1:n.90-178_90-177del
ENST00000643479.1:n.259-178_259-177del
ENST00000643516.1:c.117-178_117-177del
ENST00000644151.1:n.1344_1345del
ENST00000644218.1:c.230-178_230-177del ENSP00000493574.1:n.230-178_230-177del
ENST00000644683.1:c.230-178_230-177del ENSP00000494085.1:n.230-178_230-177del
ENST00000644810.1:c.230-801_230-800del ENSP00000495895.1:n.230-801_230-800del
ENST00000644831.1:n.259-178_259-177del
ENST00000644933.1:c.-500-178_-500-177del ENSP00000496133.1:n.-500-178_-500-177del
ENST00000645020.1:n.1080_1081del
ENST00000645285.1:c.-500-178_-500-177del ENSP00000495058.1:n.-500-178_-500-177del
ENST00000645331.1:n.252-178_252-177del
ENST00000645620.1:c.-442-178_-442-177del ENSP00000493657.1:n.-442-178_-442-177del
ENST00000646777.1:n.259-178_259-177del
ENST00000647016.1:n.385_386del
ENST00000647152.1:c.-500-178_-500-177del ENSP00000495893.1:n.-500-178_-500-177del
ENST00000647209.1:c.*99-178_*99-177del ENSP00000495558.1:n.*99-178_*99-177del
ENST00000647346.1:n.1072_1073del
ENST00000299427.10:c.230-178_230-177del ENSP00000299427.6:n.230-178_230-177del
ENST00000428886.6:n.252-178_252-177del
ENST00000436873.6:c.230-178_230-177del ENSP00000398136.2:n.230-178_230-177del
ENST00000528571.5:c.90-178_90-177del ENSP00000434647.1:n.90-178_90-177del
ENST00000528917.1:n.531-178_531-177del
ENST00000530040.1:n.342-178_342-177del
ENST00000533371.5:c.-500-178_-500-177del ENSP00000437066.1:n.-500-178_-500-177del
ENST00000534644.5:n.215-178_215-177del
ENST00000611494.4:c.230-178_230-177del ENSP00000484546.1:n.230-178_230-177del
NM_000391.3:c.230-178_230-177del NP_000382.3:n.230-178_230-177del
NM_000391.4:c.230-178_230-177del MANE Select NP_000382.3:n.230-178_230-177del