Canonical Allele Identifier: CA2790314479

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617995_6617996insA , CM000673.2:g.6617995_6617996insA	GRCh38
NC_000011.9:g.6639226_6639227insA , CM000673.1:g.6639226_6639227insA	GRCh37
NC_000011.8:g.6595802_6595803insA	NCBI36
NG_008653.1:g.6466_6467insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.116-220_116-219insT	ENSP00000507321.1:n.116-220_116-219insT
ENST00000299427.12:c.230-220_230-219insT MANE Select	ENSP00000299427.6:n.230-220_230-219insT
ENST00000428886.7:n.318-220_318-219insT
ENST00000436873.7:c.34-220_34-219insT
ENST00000524788.2:n.1022_1023insT
ENST00000524903.2:n.1138_1139insT
ENST00000528571.6:c.90-220_90-219insT	ENSP00000434647.1:n.90-220_90-219insT
ENST00000530040.2:n.259-220_259-219insT
ENST00000533371.6:c.-500-220_-500-219insT	ENSP00000437066.1:n.-500-220_-500-219insT
ENST00000534644.6:n.231-220_231-219insT
ENST00000642892.1:c.-447-220_-447-219insT	ENSP00000494165.1:n.-447-220_-447-219insT
ENST00000643439.1:c.90-220_90-219insT	ENSP00000495849.1:n.90-220_90-219insT
ENST00000643479.1:n.259-220_259-219insT
ENST00000643516.1:c.117-220_117-219insT
ENST00000644151.1:n.1302_1303insT
ENST00000644218.1:c.230-220_230-219insT	ENSP00000493574.1:n.230-220_230-219insT
ENST00000644683.1:c.230-220_230-219insT	ENSP00000494085.1:n.230-220_230-219insT
ENST00000644810.1:c.229+780_229+781insT	ENSP00000495895.1:n.229+780_229+781insT
ENST00000644831.1:n.259-220_259-219insT
ENST00000644933.1:c.-500-220_-500-219insT	ENSP00000496133.1:n.-500-220_-500-219insT
ENST00000645020.1:n.1038_1039insT
ENST00000645285.1:c.-500-220_-500-219insT	ENSP00000495058.1:n.-500-220_-500-219insT
ENST00000645331.1:n.252-220_252-219insT
ENST00000645620.1:c.-442-220_-442-219insT	ENSP00000493657.1:n.-442-220_-442-219insT
ENST00000646777.1:n.259-220_259-219insT
ENST00000647016.1:n.343_344insT
ENST00000647152.1:c.-500-220_-500-219insT	ENSP00000495893.1:n.-500-220_-500-219insT
ENST00000647209.1:c.*99-220_*99-219insT	ENSP00000495558.1:n.*99-220_*99-219insT
ENST00000647346.1:n.1030_1031insT
ENST00000299427.10:c.230-220_230-219insT	ENSP00000299427.6:n.230-220_230-219insT
ENST00000428886.6:n.252-220_252-219insT
ENST00000436873.6:c.230-220_230-219insT	ENSP00000398136.2:n.230-220_230-219insT
ENST00000528571.5:c.90-220_90-219insT	ENSP00000434647.1:n.90-220_90-219insT
ENST00000528917.1:n.531-220_531-219insT
ENST00000530040.1:n.342-220_342-219insT
ENST00000533371.5:c.-500-220_-500-219insT	ENSP00000437066.1:n.-500-220_-500-219insT
ENST00000534644.5:n.215-220_215-219insT
ENST00000611494.4:c.230-220_230-219insT	ENSP00000484546.1:n.230-220_230-219insT
NM_000391.3:c.230-220_230-219insT	NP_000382.3:n.230-220_230-219insT
NM_000391.4:c.230-220_230-219insT MANE Select	NP_000382.3:n.230-220_230-219insT