Canonical Allele Identifier: CA2790314469

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617964_6617965insA , CM000673.2:g.6617964_6617965insA	GRCh38
NC_000011.9:g.6639195_6639196insA , CM000673.1:g.6639195_6639196insA	GRCh37
NC_000011.8:g.6595771_6595772insA	NCBI36
NG_008653.1:g.6497_6498insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.116-189_116-188insT	ENSP00000507321.1:n.116-189_116-188insT
ENST00000299427.12:c.230-189_230-188insT MANE Select	ENSP00000299427.6:n.230-189_230-188insT
ENST00000428886.7:n.318-189_318-188insT
ENST00000436873.7:c.34-189_34-188insT
ENST00000524788.2:n.1053_1054insT
ENST00000524903.2:n.1169_1170insT
ENST00000528571.6:c.90-189_90-188insT	ENSP00000434647.1:n.90-189_90-188insT
ENST00000530040.2:n.259-189_259-188insT
ENST00000533371.6:c.-500-189_-500-188insT	ENSP00000437066.1:n.-500-189_-500-188insT
ENST00000534644.6:n.231-189_231-188insT
ENST00000642892.1:c.-447-189_-447-188insT	ENSP00000494165.1:n.-447-189_-447-188insT
ENST00000643439.1:c.90-189_90-188insT	ENSP00000495849.1:n.90-189_90-188insT
ENST00000643479.1:n.259-189_259-188insT
ENST00000643516.1:c.117-189_117-188insT
ENST00000644151.1:n.1333_1334insT
ENST00000644218.1:c.230-189_230-188insT	ENSP00000493574.1:n.230-189_230-188insT
ENST00000644683.1:c.230-189_230-188insT	ENSP00000494085.1:n.230-189_230-188insT
ENST00000644810.1:c.230-812_230-811insT	ENSP00000495895.1:n.230-812_230-811insT
ENST00000644831.1:n.259-189_259-188insT
ENST00000644933.1:c.-500-189_-500-188insT	ENSP00000496133.1:n.-500-189_-500-188insT
ENST00000645020.1:n.1069_1070insT
ENST00000645285.1:c.-500-189_-500-188insT	ENSP00000495058.1:n.-500-189_-500-188insT
ENST00000645331.1:n.252-189_252-188insT
ENST00000645620.1:c.-442-189_-442-188insT	ENSP00000493657.1:n.-442-189_-442-188insT
ENST00000646777.1:n.259-189_259-188insT
ENST00000647016.1:n.374_375insT
ENST00000647152.1:c.-500-189_-500-188insT	ENSP00000495893.1:n.-500-189_-500-188insT
ENST00000647209.1:c.*99-189_*99-188insT	ENSP00000495558.1:n.*99-189_*99-188insT
ENST00000647346.1:n.1061_1062insT
ENST00000299427.10:c.230-189_230-188insT	ENSP00000299427.6:n.230-189_230-188insT
ENST00000428886.6:n.252-189_252-188insT
ENST00000436873.6:c.230-189_230-188insT	ENSP00000398136.2:n.230-189_230-188insT
ENST00000528571.5:c.90-189_90-188insT	ENSP00000434647.1:n.90-189_90-188insT
ENST00000528917.1:n.531-189_531-188insT
ENST00000530040.1:n.342-189_342-188insT
ENST00000533371.5:c.-500-189_-500-188insT	ENSP00000437066.1:n.-500-189_-500-188insT
ENST00000534644.5:n.215-189_215-188insT
ENST00000611494.4:c.230-189_230-188insT	ENSP00000484546.1:n.230-189_230-188insT
NM_000391.3:c.230-189_230-188insT	NP_000382.3:n.230-189_230-188insT
NM_000391.4:c.230-189_230-188insT MANE Select	NP_000382.3:n.230-189_230-188insT