Canonical Allele Identifier: CA1950237960
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617082C= , CM000673.2:g.6617082C= GRCh38
NC_000011.9:g.6638313C= , CM000673.1:g.6638313C= GRCh37
NC_000011.8:g.6594889C= NCBI36
NG_008653.1:g.7380G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.466G= ENSP00000507321.1:p.Val156=
ENST00000299427.12:c.580G= MANE Select ENSP00000299427.6:p.Val194=
ENST00000428886.7:n.815G=
ENST00000436873.7:c.312+219G=
ENST00000524788.2:n.1739G=
ENST00000524903.2:n.1855G=
ENST00000528807.2:n.236G=
ENST00000530040.2:n.479+277G=
ENST00000533371.6:c.-150G= ENSP00000437066.1:n.-150G=
ENST00000534644.6:n.528G=
ENST00000642892.1:c.-150G= ENSP00000494165.1:n.-150G=
ENST00000643439.1:c.*320G= ENSP00000495849.1:n.*320G=
ENST00000643479.1:n.609G=
ENST00000643516.1:c.395+219G=
ENST00000644151.1:n.2019G=
ENST00000644218.1:c.580G= ENSP00000493574.1:p.Val194=
ENST00000644683.1:c.*33G= ENSP00000494085.1:n.*33G=
ENST00000644810.1:c.301G= ENSP00000495895.1:p.Val101=
ENST00000644831.1:n.756G=
ENST00000644933.1:c.-150G= ENSP00000496133.1:n.-150G=
ENST00000645020.1:n.1755G=
ENST00000645285.1:c.-150G= ENSP00000495058.1:n.-150G=
ENST00000645331.1:n.946G=
ENST00000645620.1:c.-150G= ENSP00000493657.1:n.-150G=
ENST00000646777.1:n.756G=
ENST00000647016.1:n.1060G=
ENST00000647152.1:c.-150G= ENSP00000495893.1:n.-150G=
ENST00000647209.1:c.*449G= ENSP00000495558.1:n.*449G=
ENST00000647346.1:n.1600G=
ENST00000299427.10:c.580G= ENSP00000299427.6:p.Val194=
ENST00000428886.6:n.749G=
ENST00000436873.6:c.450+277G= ENSP00000398136.2:n.450+277G=
ENST00000524788.1:n.280G=
ENST00000528571.5:c.*320G= ENSP00000434647.1:n.*320G=
ENST00000528807.1:n.130G=
ENST00000533371.5:c.-150G= ENSP00000437066.1:n.-150G=
ENST00000534644.5:n.565G=
ENST00000611494.4:c.580G= ENSP00000484546.1:p.Val194=
NM_000391.3:c.580G= NP_000382.3:p.Val194=
NM_000391.4:c.580G= MANE Select NP_000382.3:p.Val194=