Canonical Allele Identifier: CA1950237842
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617039C= , CM000673.2:g.6617039C= GRCh38
NC_000011.9:g.6638270C= , CM000673.1:g.6638270C= GRCh37
NC_000011.8:g.6594846C= NCBI36
NG_008653.1:g.7423G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.509G= ENSP00000507321.1:p.Arg170=
ENST00000299427.12:c.623G= MANE Select ENSP00000299427.6:p.Arg208=
ENST00000436873.7:c.312+262G=
ENST00000524788.2:n.1782G=
ENST00000524903.2:n.1898G=
ENST00000528807.2:n.279G=
ENST00000530040.2:n.479+320G=
ENST00000533371.6:c.-107G= ENSP00000437066.1:n.-107G=
ENST00000534644.6:n.571G=
ENST00000642892.1:c.-107G= ENSP00000494165.1:n.-107G=
ENST00000643439.1:c.*363G= ENSP00000495849.1:n.*363G=
ENST00000643479.1:n.652G=
ENST00000643516.1:c.395+262G=
ENST00000644151.1:n.2062G=
ENST00000644218.1:c.623G= ENSP00000493574.1:p.Arg208=
ENST00000644683.1:c.*76G= ENSP00000494085.1:n.*76G=
ENST00000644810.1:c.344G= ENSP00000495895.1:p.Arg115=
ENST00000644831.1:n.799G=
ENST00000644933.1:c.-107G= ENSP00000496133.1:n.-107G=
ENST00000645020.1:n.1798G=
ENST00000645285.1:c.-107G= ENSP00000495058.1:n.-107G=
ENST00000645331.1:n.989G=
ENST00000645620.1:c.-107G= ENSP00000493657.1:n.-107G=
ENST00000646777.1:n.799G=
ENST00000647016.1:n.1103G=
ENST00000647152.1:c.-107G= ENSP00000495893.1:n.-107G=
ENST00000647209.1:c.*492G= ENSP00000495558.1:n.*492G=
ENST00000647346.1:n.1643G=
ENST00000299427.10:c.623G= ENSP00000299427.6:p.Arg208=
ENST00000428886.6:n.792G=
ENST00000436873.6:c.450+320G= ENSP00000398136.2:n.450+320G=
ENST00000524788.1:n.323G=
ENST00000528571.5:c.*363G= ENSP00000434647.1:n.*363G=
ENST00000528807.1:n.173G=
ENST00000533371.5:c.-107G= ENSP00000437066.1:n.-107G=
ENST00000534644.5:n.608G=
ENST00000611494.4:c.623G= ENSP00000484546.1:p.Arg208=
NM_000391.3:c.623G= NP_000382.3:p.Arg208=
NM_000391.4:c.623G= MANE Select NP_000382.3:p.Arg208=