Canonical Allele Identifier: CA1950214798
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617305G= , CM000673.2:g.6617305G= GRCh38
NC_000011.9:g.6638536G= , CM000673.1:g.6638536G= GRCh37
NC_000011.8:g.6595112G= NCBI36
NG_008653.1:g.7157C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.390C= ENSP00000507321.1:p.Asp130=
ENST00000299427.12:c.504C= MANE Select ENSP00000299427.6:p.Asp168=
ENST00000428886.7:n.592C=
ENST00000436873.7:c.308C=
ENST00000524788.2:n.1516C=
ENST00000524903.2:n.1632C=
ENST00000528571.6:c.*244C= ENSP00000434647.1:n.*244C=
ENST00000528807.2:n.160C=
ENST00000530040.2:n.479+54C=
ENST00000533371.6:c.-226C= ENSP00000437066.1:n.-226C=
ENST00000534644.6:n.456+49C=
ENST00000642892.1:c.-222+49C= ENSP00000494165.1:n.-222+49C=
ENST00000643439.1:c.*244C= ENSP00000495849.1:n.*244C=
ENST00000643479.1:n.533C=
ENST00000643516.1:c.391C=
ENST00000644151.1:n.1796C=
ENST00000644218.1:c.504C= ENSP00000493574.1:p.Asp168=
ENST00000644683.1:c.450+54C= ENSP00000494085.1:n.450+54C=
ENST00000644810.1:c.230-152C= ENSP00000495895.1:n.230-152C=
ENST00000644831.1:n.533C=
ENST00000644933.1:c.-226C= ENSP00000496133.1:n.-226C=
ENST00000645020.1:n.1532C=
ENST00000645285.1:c.-226C= ENSP00000495058.1:n.-226C=
ENST00000645331.1:n.723C=
ENST00000645620.1:c.-222+54C= ENSP00000493657.1:n.-222+54C=
ENST00000646777.1:n.533C=
ENST00000647016.1:n.837C=
ENST00000647152.1:c.-226C= ENSP00000495893.1:n.-226C=
ENST00000647209.1:c.*373C= ENSP00000495558.1:n.*373C=
ENST00000647346.1:n.1524C=
ENST00000299427.10:c.504C= ENSP00000299427.6:p.Asp168=
ENST00000428886.6:n.526C=
ENST00000436873.6:c.450+54C= ENSP00000398136.2:n.450+54C=
ENST00000524788.1:n.57C=
ENST00000528571.5:c.*244C= ENSP00000434647.1:n.*244C=
ENST00000533371.5:c.-226C= ENSP00000437066.1:n.-226C=
ENST00000534644.5:n.489C=
ENST00000611494.4:c.504C= ENSP00000484546.1:p.Asp168=
NM_000391.3:c.504C= NP_000382.3:p.Asp168=
NM_000391.4:c.504C= MANE Select NP_000382.3:p.Asp168=