Canonical Allele Identifier: CA2790314238

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616094_6616095insA , CM000673.2:g.6616094_6616095insA	GRCh38
NC_000011.9:g.6637325_6637326insA , CM000673.1:g.6637325_6637326insA	GRCh37
NC_000011.8:g.6593901_6593902insA	NCBI36
NG_008653.1:g.8367_8368insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.962-21_962-20insT	ENSP00000507321.1:n.962-21_962-20insT
ENST00000299427.12:c.1076-21_1076-20insT MANE Select	ENSP00000299427.6:n.1076-21_1076-20insT
ENST00000436873.7:c.313-21_313-20insT
ENST00000524924.2:n.175_176insT
ENST00000533371.6:c.347-21_347-20insT	ENSP00000437066.1:n.347-21_347-20insT
ENST00000642892.1:c.347-21_347-20insT	ENSP00000494165.1:n.347-21_347-20insT
ENST00000643342.1:c.166-21_166-20insT
ENST00000643439.1:c.*816-21_*816-20insT	ENSP00000495849.1:n.*816-21_*816-20insT
ENST00000643479.1:n.1262-21_1262-20insT
ENST00000643516.1:c.585-21_585-20insT
ENST00000644218.1:c.887-21_887-20insT	ENSP00000493574.1:n.887-21_887-20insT
ENST00000644683.1:c.*529-21_*529-20insT	ENSP00000494085.1:n.*529-21_*529-20insT
ENST00000644810.1:c.797-21_797-20insT	ENSP00000495895.1:n.797-21_797-20insT
ENST00000644831.1:n.1252-21_1252-20insT
ENST00000644933.1:c.347-21_347-20insT	ENSP00000496133.1:n.347-21_347-20insT
ENST00000645285.1:c.158-21_158-20insT	ENSP00000495058.1:n.158-21_158-20insT
ENST00000645331.1:n.1818_1819insT
ENST00000645620.1:c.347-21_347-20insT	ENSP00000493657.1:n.347-21_347-20insT
ENST00000646691.1:n.388_389insT
ENST00000646777.1:n.1409-21_1409-20insT
ENST00000647016.1:n.1556-21_1556-20insT
ENST00000647152.1:c.347-21_347-20insT	ENSP00000495893.1:n.347-21_347-20insT
ENST00000647209.1:c.*945-21_*945-20insT	ENSP00000495558.1:n.*945-21_*945-20insT
ENST00000647346.1:n.2096-21_2096-20insT
ENST00000299427.10:c.1076-21_1076-20insT	ENSP00000299427.6:n.1076-21_1076-20insT
ENST00000524924.1:n.10_11insT
ENST00000533371.5:c.347-21_347-20insT	ENSP00000437066.1:n.347-21_347-20insT
ENST00000611494.4:c.1076-21_1076-20insT	ENSP00000484546.1:n.1076-21_1076-20insT
NM_000391.3:c.1076-21_1076-20insT	NP_000382.3:n.1076-21_1076-20insT
NM_000391.4:c.1076-21_1076-20insT MANE Select	NP_000382.3:n.1076-21_1076-20insT