Canonical Allele Identifier: CA2790314405

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617891_6617892insA , CM000673.2:g.6617891_6617892insA	GRCh38
NC_000011.9:g.6639122_6639123insA , CM000673.1:g.6639122_6639123insA	GRCh37
NC_000011.8:g.6595698_6595699insA	NCBI36
NG_008653.1:g.6570_6571insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.116-116_116-115insT	ENSP00000507321.1:n.116-116_116-115insT
ENST00000299427.12:c.230-116_230-115insT MANE Select	ENSP00000299427.6:n.230-116_230-115insT
ENST00000428886.7:n.318-116_318-115insT
ENST00000436873.7:c.34-116_34-115insT
ENST00000524788.2:n.1126_1127insT
ENST00000524903.2:n.1242_1243insT
ENST00000528571.6:c.90-116_90-115insT	ENSP00000434647.1:n.90-116_90-115insT
ENST00000530040.2:n.259-116_259-115insT
ENST00000533371.6:c.-500-116_-500-115insT	ENSP00000437066.1:n.-500-116_-500-115insT
ENST00000534644.6:n.231-116_231-115insT
ENST00000642892.1:c.-447-116_-447-115insT	ENSP00000494165.1:n.-447-116_-447-115insT
ENST00000643439.1:c.90-116_90-115insT	ENSP00000495849.1:n.90-116_90-115insT
ENST00000643479.1:n.259-116_259-115insT
ENST00000643516.1:c.117-116_117-115insT
ENST00000644151.1:n.1406_1407insT
ENST00000644218.1:c.230-116_230-115insT	ENSP00000493574.1:n.230-116_230-115insT
ENST00000644683.1:c.230-116_230-115insT	ENSP00000494085.1:n.230-116_230-115insT
ENST00000644810.1:c.230-739_230-738insT	ENSP00000495895.1:n.230-739_230-738insT
ENST00000644831.1:n.259-116_259-115insT
ENST00000644933.1:c.-500-116_-500-115insT	ENSP00000496133.1:n.-500-116_-500-115insT
ENST00000645020.1:n.1142_1143insT
ENST00000645285.1:c.-500-116_-500-115insT	ENSP00000495058.1:n.-500-116_-500-115insT
ENST00000645331.1:n.252-116_252-115insT
ENST00000645620.1:c.-442-116_-442-115insT	ENSP00000493657.1:n.-442-116_-442-115insT
ENST00000646777.1:n.259-116_259-115insT
ENST00000647016.1:n.447_448insT
ENST00000647152.1:c.-500-116_-500-115insT	ENSP00000495893.1:n.-500-116_-500-115insT
ENST00000647209.1:c.*99-116_*99-115insT	ENSP00000495558.1:n.*99-116_*99-115insT
ENST00000647346.1:n.1134_1135insT
ENST00000299427.10:c.230-116_230-115insT	ENSP00000299427.6:n.230-116_230-115insT
ENST00000428886.6:n.252-116_252-115insT
ENST00000436873.6:c.230-116_230-115insT	ENSP00000398136.2:n.230-116_230-115insT
ENST00000528571.5:c.90-116_90-115insT	ENSP00000434647.1:n.90-116_90-115insT
ENST00000528917.1:n.531-116_531-115insT
ENST00000530040.1:n.342-116_342-115insT
ENST00000533371.5:c.-500-116_-500-115insT	ENSP00000437066.1:n.-500-116_-500-115insT
ENST00000534644.5:n.215-116_215-115insT
ENST00000611494.4:c.230-116_230-115insT	ENSP00000484546.1:n.230-116_230-115insT
NM_000391.3:c.230-116_230-115insT	NP_000382.3:n.230-116_230-115insT
NM_000391.4:c.230-116_230-115insT MANE Select	NP_000382.3:n.230-116_230-115insT