Canonical Allele Identifier: CA2790314470
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617966_6617968del , CM000673.2:g.6617966_6617968del GRCh38
NC_000011.9:g.6639197_6639199del , CM000673.1:g.6639197_6639199del GRCh37
NC_000011.8:g.6595773_6595775del NCBI36
NG_008653.1:g.6494_6496del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-192_116-190del ENSP00000507321.1:n.116-192_116-190del
ENST00000299427.12:c.230-192_230-190del MANE Select ENSP00000299427.6:n.230-192_230-190del
ENST00000428886.7:n.318-192_318-190del
ENST00000436873.7:c.34-192_34-190del
ENST00000524788.2:n.1050_1052del
ENST00000524903.2:n.1166_1168del
ENST00000528571.6:c.90-192_90-190del ENSP00000434647.1:n.90-192_90-190del
ENST00000530040.2:n.259-192_259-190del
ENST00000533371.6:c.-500-192_-500-190del ENSP00000437066.1:n.-500-192_-500-190del
ENST00000534644.6:n.231-192_231-190del
ENST00000642892.1:c.-447-192_-447-190del ENSP00000494165.1:n.-447-192_-447-190del
ENST00000643439.1:c.90-192_90-190del ENSP00000495849.1:n.90-192_90-190del
ENST00000643479.1:n.259-192_259-190del
ENST00000643516.1:c.117-192_117-190del
ENST00000644151.1:n.1330_1332del
ENST00000644218.1:c.230-192_230-190del ENSP00000493574.1:n.230-192_230-190del
ENST00000644683.1:c.230-192_230-190del ENSP00000494085.1:n.230-192_230-190del
ENST00000644810.1:c.229+808_229+810del ENSP00000495895.1:n.229+808_229+810del
ENST00000644831.1:n.259-192_259-190del
ENST00000644933.1:c.-500-192_-500-190del ENSP00000496133.1:n.-500-192_-500-190del
ENST00000645020.1:n.1066_1068del
ENST00000645285.1:c.-500-192_-500-190del ENSP00000495058.1:n.-500-192_-500-190del
ENST00000645331.1:n.252-192_252-190del
ENST00000645620.1:c.-442-192_-442-190del ENSP00000493657.1:n.-442-192_-442-190del
ENST00000646777.1:n.259-192_259-190del
ENST00000647016.1:n.371_373del
ENST00000647152.1:c.-500-192_-500-190del ENSP00000495893.1:n.-500-192_-500-190del
ENST00000647209.1:c.*99-192_*99-190del ENSP00000495558.1:n.*99-192_*99-190del
ENST00000647346.1:n.1058_1060del
ENST00000299427.10:c.230-192_230-190del ENSP00000299427.6:n.230-192_230-190del
ENST00000428886.6:n.252-192_252-190del
ENST00000436873.6:c.230-192_230-190del ENSP00000398136.2:n.230-192_230-190del
ENST00000528571.5:c.90-192_90-190del ENSP00000434647.1:n.90-192_90-190del
ENST00000528917.1:n.531-192_531-190del
ENST00000530040.1:n.342-192_342-190del
ENST00000533371.5:c.-500-192_-500-190del ENSP00000437066.1:n.-500-192_-500-190del
ENST00000534644.5:n.215-192_215-190del
ENST00000611494.4:c.230-192_230-190del ENSP00000484546.1:n.230-192_230-190del
NM_000391.3:c.230-192_230-190del NP_000382.3:n.230-192_230-190del
NM_000391.4:c.230-192_230-190del MANE Select NP_000382.3:n.230-192_230-190del