Canonical Allele Identifier: CA2790314428

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617915_6617916insA , CM000673.2:g.6617915_6617916insA	GRCh38
NC_000011.9:g.6639146_6639147insA , CM000673.1:g.6639146_6639147insA	GRCh37
NC_000011.8:g.6595722_6595723insA	NCBI36
NG_008653.1:g.6546_6547insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.116-140_116-139insT	ENSP00000507321.1:n.116-140_116-139insT
ENST00000299427.12:c.230-140_230-139insT MANE Select	ENSP00000299427.6:n.230-140_230-139insT
ENST00000428886.7:n.318-140_318-139insT
ENST00000436873.7:c.34-140_34-139insT
ENST00000524788.2:n.1102_1103insT
ENST00000524903.2:n.1218_1219insT
ENST00000528571.6:c.90-140_90-139insT	ENSP00000434647.1:n.90-140_90-139insT
ENST00000530040.2:n.259-140_259-139insT
ENST00000533371.6:c.-500-140_-500-139insT	ENSP00000437066.1:n.-500-140_-500-139insT
ENST00000534644.6:n.231-140_231-139insT
ENST00000642892.1:c.-447-140_-447-139insT	ENSP00000494165.1:n.-447-140_-447-139insT
ENST00000643439.1:c.90-140_90-139insT	ENSP00000495849.1:n.90-140_90-139insT
ENST00000643479.1:n.259-140_259-139insT
ENST00000643516.1:c.117-140_117-139insT
ENST00000644151.1:n.1382_1383insT
ENST00000644218.1:c.230-140_230-139insT	ENSP00000493574.1:n.230-140_230-139insT
ENST00000644683.1:c.230-140_230-139insT	ENSP00000494085.1:n.230-140_230-139insT
ENST00000644810.1:c.230-763_230-762insT	ENSP00000495895.1:n.230-763_230-762insT
ENST00000644831.1:n.259-140_259-139insT
ENST00000644933.1:c.-500-140_-500-139insT	ENSP00000496133.1:n.-500-140_-500-139insT
ENST00000645020.1:n.1118_1119insT
ENST00000645285.1:c.-500-140_-500-139insT	ENSP00000495058.1:n.-500-140_-500-139insT
ENST00000645331.1:n.252-140_252-139insT
ENST00000645620.1:c.-442-140_-442-139insT	ENSP00000493657.1:n.-442-140_-442-139insT
ENST00000646777.1:n.259-140_259-139insT
ENST00000647016.1:n.423_424insT
ENST00000647152.1:c.-500-140_-500-139insT	ENSP00000495893.1:n.-500-140_-500-139insT
ENST00000647209.1:c.*99-140_*99-139insT	ENSP00000495558.1:n.*99-140_*99-139insT
ENST00000647346.1:n.1110_1111insT
ENST00000299427.10:c.230-140_230-139insT	ENSP00000299427.6:n.230-140_230-139insT
ENST00000428886.6:n.252-140_252-139insT
ENST00000436873.6:c.230-140_230-139insT	ENSP00000398136.2:n.230-140_230-139insT
ENST00000528571.5:c.90-140_90-139insT	ENSP00000434647.1:n.90-140_90-139insT
ENST00000528917.1:n.531-140_531-139insT
ENST00000530040.1:n.342-140_342-139insT
ENST00000533371.5:c.-500-140_-500-139insT	ENSP00000437066.1:n.-500-140_-500-139insT
ENST00000534644.5:n.215-140_215-139insT
ENST00000611494.4:c.230-140_230-139insT	ENSP00000484546.1:n.230-140_230-139insT
NM_000391.3:c.230-140_230-139insT	NP_000382.3:n.230-140_230-139insT
NM_000391.4:c.230-140_230-139insT MANE Select	NP_000382.3:n.230-140_230-139insT