Canonical Allele Identifier: CA2790314464

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617959_6617960insAC , CM000673.2:g.6617959_6617960insAC	GRCh38
NC_000011.9:g.6639190_6639191insAC , CM000673.1:g.6639190_6639191insAC	GRCh37
NC_000011.8:g.6595766_6595767insAC	NCBI36
NG_008653.1:g.6502_6503insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.116-184_116-183insGT	ENSP00000507321.1:n.116-184_116-183insGT
ENST00000299427.12:c.230-184_230-183insGT MANE Select	ENSP00000299427.6:n.230-184_230-183insGT
ENST00000428886.7:n.318-184_318-183insGT
ENST00000436873.7:c.34-184_34-183insGT
ENST00000524788.2:n.1058_1059insGT
ENST00000524903.2:n.1174_1175insGT
ENST00000528571.6:c.90-184_90-183insGT	ENSP00000434647.1:n.90-184_90-183insGT
ENST00000530040.2:n.259-184_259-183insGT
ENST00000533371.6:c.-500-184_-500-183insGT	ENSP00000437066.1:n.-500-184_-500-183insGT
ENST00000534644.6:n.231-184_231-183insGT
ENST00000642892.1:c.-447-184_-447-183insGT	ENSP00000494165.1:n.-447-184_-447-183insGT
ENST00000643439.1:c.90-184_90-183insGT	ENSP00000495849.1:n.90-184_90-183insGT
ENST00000643479.1:n.259-184_259-183insGT
ENST00000643516.1:c.117-184_117-183insGT
ENST00000644151.1:n.1338_1339insGT
ENST00000644218.1:c.230-184_230-183insGT	ENSP00000493574.1:n.230-184_230-183insGT
ENST00000644683.1:c.230-184_230-183insGT	ENSP00000494085.1:n.230-184_230-183insGT
ENST00000644810.1:c.230-807_230-806insGT	ENSP00000495895.1:n.230-807_230-806insGT
ENST00000644831.1:n.259-184_259-183insGT
ENST00000644933.1:c.-500-184_-500-183insGT	ENSP00000496133.1:n.-500-184_-500-183insGT
ENST00000645020.1:n.1074_1075insGT
ENST00000645285.1:c.-500-184_-500-183insGT	ENSP00000495058.1:n.-500-184_-500-183insGT
ENST00000645331.1:n.252-184_252-183insGT
ENST00000645620.1:c.-442-184_-442-183insGT	ENSP00000493657.1:n.-442-184_-442-183insGT
ENST00000646777.1:n.259-184_259-183insGT
ENST00000647016.1:n.379_380insGT
ENST00000647152.1:c.-500-184_-500-183insGT	ENSP00000495893.1:n.-500-184_-500-183insGT
ENST00000647209.1:c.*99-184_*99-183insGT	ENSP00000495558.1:n.*99-184_*99-183insGT
ENST00000647346.1:n.1066_1067insGT
ENST00000299427.10:c.230-184_230-183insGT	ENSP00000299427.6:n.230-184_230-183insGT
ENST00000428886.6:n.252-184_252-183insGT
ENST00000436873.6:c.230-184_230-183insGT	ENSP00000398136.2:n.230-184_230-183insGT
ENST00000528571.5:c.90-184_90-183insGT	ENSP00000434647.1:n.90-184_90-183insGT
ENST00000528917.1:n.531-184_531-183insGT
ENST00000530040.1:n.342-184_342-183insGT
ENST00000533371.5:c.-500-184_-500-183insGT	ENSP00000437066.1:n.-500-184_-500-183insGT
ENST00000534644.5:n.215-184_215-183insGT
ENST00000611494.4:c.230-184_230-183insGT	ENSP00000484546.1:n.230-184_230-183insGT
NM_000391.3:c.230-184_230-183insGT	NP_000382.3:n.230-184_230-183insGT
NM_000391.4:c.230-184_230-183insGT MANE Select	NP_000382.3:n.230-184_230-183insGT