Canonical Allele Identifier: CA645575504

Gene: TPP1

Linked Data

• COSMIC: COSM5201251

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617406del , CM000673.2:g.6617406del	GRCh38
NC_000011.9:g.6638637del , CM000673.1:g.6638637del	GRCh37
NC_000011.8:g.6595213del	NCBI36
NG_008653.1:g.7059del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.292del	ENSP00000507321.1:p.Ala98LeufsTer16
ENST00000299427.12:c.406del MANE Select	ENSP00000299427.6:p.Ala136LeufsTer16
ENST00000428886.7:n.494del
ENST00000436873.7:c.210del
ENST00000524788.2:n.1418del
ENST00000524903.2:n.1534del
ENST00000528571.6:c.*146del	ENSP00000434647.1:n.*146del
ENST00000528807.2:n.62del
ENST00000530040.2:n.435del
ENST00000533371.6:c.-324del	ENSP00000437066.1:n.-324del
ENST00000534644.6:n.407del
ENST00000642892.1:c.-271del	ENSP00000494165.1:n.-271del
ENST00000643439.1:c.*146del	ENSP00000495849.1:n.*146del
ENST00000643479.1:n.435del
ENST00000643516.1:c.293del
ENST00000644151.1:n.1698del
ENST00000644218.1:c.406del	ENSP00000493574.1:p.Ala136LeufsTer16
ENST00000644683.1:c.406del	ENSP00000494085.1:p.Ala136LeufsTer?
ENST00000644810.1:c.230-250del	ENSP00000495895.1:n.230-250del
ENST00000644831.1:n.435del
ENST00000644933.1:c.-324del	ENSP00000496133.1:n.-324del
ENST00000645020.1:n.1434del
ENST00000645285.1:c.-324del	ENSP00000495058.1:n.-324del
ENST00000645331.1:n.625del
ENST00000645620.1:c.-266del	ENSP00000493657.1:n.-266del
ENST00000646777.1:n.435del
ENST00000647016.1:n.739del
ENST00000647152.1:c.-324del	ENSP00000495893.1:n.-324del
ENST00000647209.1:c.*275del	ENSP00000495558.1:n.*275del
ENST00000647346.1:n.1426del
ENST00000299427.10:c.406del	ENSP00000299427.6:p.Ala136LeufsTer16
ENST00000428886.6:n.428del
ENST00000436873.6:c.406del	ENSP00000398136.2:p.Ala136LeufsTer18
ENST00000528571.5:c.*146del	ENSP00000434647.1:n.*146del
ENST00000530040.1:n.518del
ENST00000533371.5:c.-324del	ENSP00000437066.1:n.-324del
ENST00000534644.5:n.391del
ENST00000611494.4:c.406del	ENSP00000484546.1:p.Ala136LeufsTer16
NM_000391.3:c.406del	NP_000382.3:p.Ala136LeufsTer16
NM_000391.4:c.406del MANE Select	NP_000382.3:p.Ala136LeufsTer16