Canonical Allele Identifier: CA1950215365
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617736C= , CM000673.2:g.6617736C= GRCh38
NC_000011.9:g.6638967C= , CM000673.1:g.6638967C= GRCh37
NC_000011.8:g.6595543C= NCBI36
NG_008653.1:g.6726G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.156G= ENSP00000507321.1:p.Arg52=
ENST00000299427.12:c.270G= MANE Select ENSP00000299427.6:p.Arg90=
ENST00000428886.7:n.358G=
ENST00000436873.7:c.74G=
ENST00000524788.2:n.1282G=
ENST00000524903.2:n.1398G=
ENST00000528571.6:c.*10G= ENSP00000434647.1:n.*10G=
ENST00000530040.2:n.299G=
ENST00000533371.6:c.-460G= ENSP00000437066.1:n.-460G=
ENST00000534644.6:n.271G=
ENST00000642892.1:c.-407G= ENSP00000494165.1:n.-407G=
ENST00000643439.1:c.*10G= ENSP00000495849.1:n.*10G=
ENST00000643479.1:n.299G=
ENST00000643516.1:c.157G=
ENST00000644151.1:n.1562G=
ENST00000644218.1:c.270G= ENSP00000493574.1:p.Arg90=
ENST00000644683.1:c.270G= ENSP00000494085.1:p.Arg90=
ENST00000644810.1:c.230-583G= ENSP00000495895.1:n.230-583G=
ENST00000644831.1:n.299G=
ENST00000644933.1:c.-460G= ENSP00000496133.1:n.-460G=
ENST00000645020.1:n.1298G=
ENST00000645285.1:c.-460G= ENSP00000495058.1:n.-460G=
ENST00000645331.1:n.292G=
ENST00000645620.1:c.-402G= ENSP00000493657.1:n.-402G=
ENST00000646777.1:n.299G=
ENST00000647016.1:n.603G=
ENST00000647152.1:c.-460G= ENSP00000495893.1:n.-460G=
ENST00000647209.1:c.*139G= ENSP00000495558.1:n.*139G=
ENST00000647346.1:n.1290G=
ENST00000299427.10:c.270G= ENSP00000299427.6:p.Arg90=
ENST00000428886.6:n.292G=
ENST00000436873.6:c.270G= ENSP00000398136.2:p.Arg90=
ENST00000528571.5:c.*10G= ENSP00000434647.1:n.*10G=
ENST00000530040.1:n.382G=
ENST00000533371.5:c.-460G= ENSP00000437066.1:n.-460G=
ENST00000534644.5:n.255G=
ENST00000611494.4:c.270G= ENSP00000484546.1:p.Arg90=
NM_000391.3:c.270G= NP_000382.3:p.Arg90=
NM_000391.4:c.270G= MANE Select NP_000382.3:p.Arg90=