Canonical Allele Identifier: CA2790314326

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616908_6616909insA , CM000673.2:g.6616908_6616909insA	GRCh38
NC_000011.9:g.6638139_6638140insA , CM000673.1:g.6638139_6638140insA	GRCh37
NC_000011.8:g.6594715_6594716insA	NCBI36
NG_008653.1:g.7553_7554insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.574-50_574-49insT	ENSP00000507321.1:n.574-50_574-49insT
ENST00000299427.12:c.688-50_688-49insT MANE Select	ENSP00000299427.6:n.688-50_688-49insT
ENST00000436873.7:c.312+392_312+393insT
ENST00000524788.2:n.1847-50_1847-49insT
ENST00000524903.2:n.1963-50_1963-49insT
ENST00000528807.2:n.344-50_344-49insT
ENST00000530040.2:n.480-406_480-405insT
ENST00000533371.6:c.-42-50_-42-49insT	ENSP00000437066.1:n.-42-50_-42-49insT
ENST00000642892.1:c.-42-50_-42-49insT	ENSP00000494165.1:n.-42-50_-42-49insT
ENST00000643439.1:c.*428-50_*428-49insT	ENSP00000495849.1:n.*428-50_*428-49insT
ENST00000643479.1:n.717-50_717-49insT
ENST00000643516.1:c.395+392_395+393insT
ENST00000644151.1:n.2127-50_2127-49insT
ENST00000644218.1:c.688-50_688-49insT	ENSP00000493574.1:n.688-50_688-49insT
ENST00000644683.1:c.*141-50_*141-49insT	ENSP00000494085.1:n.*141-50_*141-49insT
ENST00000644810.1:c.409-50_409-49insT	ENSP00000495895.1:n.409-50_409-49insT
ENST00000644831.1:n.864-50_864-49insT
ENST00000644933.1:c.-42-50_-42-49insT	ENSP00000496133.1:n.-42-50_-42-49insT
ENST00000645020.1:n.1928_1929insT
ENST00000645285.1:c.-42-50_-42-49insT	ENSP00000495058.1:n.-42-50_-42-49insT
ENST00000645331.1:n.1054-50_1054-49insT
ENST00000645620.1:c.-42-50_-42-49insT	ENSP00000493657.1:n.-42-50_-42-49insT
ENST00000646777.1:n.864-50_864-49insT
ENST00000647016.1:n.1168-50_1168-49insT
ENST00000647152.1:c.-42-50_-42-49insT	ENSP00000495893.1:n.-42-50_-42-49insT
ENST00000647209.1:c.*557-50_*557-49insT	ENSP00000495558.1:n.*557-50_*557-49insT
ENST00000647346.1:n.1708-50_1708-49insT
ENST00000299427.10:c.688-50_688-49insT	ENSP00000299427.6:n.688-50_688-49insT
ENST00000436873.6:c.451-406_451-405insT	ENSP00000398136.2:n.451-406_451-405insT
ENST00000524788.1:n.388-50_388-49insT
ENST00000528807.1:n.238-50_238-49insT
ENST00000533371.5:c.-42-50_-42-49insT	ENSP00000437066.1:n.-42-50_-42-49insT
ENST00000611494.4:c.688-50_688-49insT	ENSP00000484546.1:n.688-50_688-49insT
NM_000391.3:c.688-50_688-49insT	NP_000382.3:n.688-50_688-49insT
NM_000391.4:c.688-50_688-49insT MANE Select	NP_000382.3:n.688-50_688-49insT