Canonical Allele Identifier: CA1950237182
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616704C= , CM000673.2:g.6616704C= GRCh38
NC_000011.9:g.6637935C= , CM000673.1:g.6637935C= GRCh37
NC_000011.8:g.6594511C= NCBI36
NG_008653.1:g.7758G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.729G= ENSP00000507321.1:p.Met243=
ENST00000299427.12:c.843G= MANE Select ENSP00000299427.6:p.Met281=
ENST00000436873.7:c.312+597G=
ENST00000524788.2:n.2002G=
ENST00000524903.2:n.2118G=
ENST00000528807.2:n.499G=
ENST00000530040.2:n.480-201G=
ENST00000533371.6:c.114G= ENSP00000437066.1:p.Met38=
ENST00000642892.1:c.114G= ENSP00000494165.1:p.Met38=
ENST00000643439.1:c.*583G= ENSP00000495849.1:n.*583G=
ENST00000643479.1:n.872G=
ENST00000643516.1:c.396-201G=
ENST00000644151.1:n.2282G=
ENST00000644218.1:c.843G= ENSP00000493574.1:p.Met281=
ENST00000644683.1:c.*296G= ENSP00000494085.1:n.*296G=
ENST00000644810.1:c.564G= ENSP00000495895.1:p.Met188=
ENST00000644831.1:n.1019G=
ENST00000644933.1:c.114G= ENSP00000496133.1:p.Met38=
ENST00000645020.1:n.2133G=
ENST00000645285.1:c.114G= ENSP00000495058.1:p.Met38=
ENST00000645331.1:n.1209G=
ENST00000645620.1:c.114G= ENSP00000493657.1:p.Met38=
ENST00000646777.1:n.1019G=
ENST00000647016.1:n.1323G=
ENST00000647152.1:c.114G= ENSP00000495893.1:p.Met38=
ENST00000647209.1:c.*712G= ENSP00000495558.1:n.*712G=
ENST00000647346.1:n.1863G=
ENST00000299427.10:c.843G= ENSP00000299427.6:p.Met281=
ENST00000436873.6:c.451-201G= ENSP00000398136.2:n.451-201G=
ENST00000524788.1:n.543G=
ENST00000528807.1:n.393G=
ENST00000533371.5:c.114G= ENSP00000437066.1:p.Met38=
ENST00000611494.4:c.843G= ENSP00000484546.1:p.Met281=
NM_000391.3:c.843G= NP_000382.3:p.Met281=
NM_000391.4:c.843G= MANE Select NP_000382.3:p.Met281=