Canonical Allele Identifier: CA1950214957
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617403C= , CM000673.2:g.6617403C= GRCh38
NC_000011.9:g.6638634C= , CM000673.1:g.6638634C= GRCh37
NC_000011.8:g.6595210C= NCBI36
NG_008653.1:g.7059G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.292G= ENSP00000507321.1:p.Ala98=
ENST00000299427.12:c.406G= MANE Select ENSP00000299427.6:p.Ala136=
ENST00000428886.7:n.494G=
ENST00000436873.7:c.210G=
ENST00000524788.2:n.1418G=
ENST00000524903.2:n.1534G=
ENST00000528571.6:c.*146G= ENSP00000434647.1:n.*146G=
ENST00000528807.2:n.62G=
ENST00000530040.2:n.435G=
ENST00000533371.6:c.-324G= ENSP00000437066.1:n.-324G=
ENST00000534644.6:n.407G=
ENST00000642892.1:c.-271G= ENSP00000494165.1:n.-271G=
ENST00000643439.1:c.*146G= ENSP00000495849.1:n.*146G=
ENST00000643479.1:n.435G=
ENST00000643516.1:c.293G=
ENST00000644151.1:n.1698G=
ENST00000644218.1:c.406G= ENSP00000493574.1:p.Ala136=
ENST00000644683.1:c.406G= ENSP00000494085.1:p.Ala136=
ENST00000644810.1:c.230-250G= ENSP00000495895.1:n.230-250G=
ENST00000644831.1:n.435G=
ENST00000644933.1:c.-324G= ENSP00000496133.1:n.-324G=
ENST00000645020.1:n.1434G=
ENST00000645285.1:c.-324G= ENSP00000495058.1:n.-324G=
ENST00000645331.1:n.625G=
ENST00000645620.1:c.-266G= ENSP00000493657.1:n.-266G=
ENST00000646777.1:n.435G=
ENST00000647016.1:n.739G=
ENST00000647152.1:c.-324G= ENSP00000495893.1:n.-324G=
ENST00000647209.1:c.*275G= ENSP00000495558.1:n.*275G=
ENST00000647346.1:n.1426G=
ENST00000299427.10:c.406G= ENSP00000299427.6:p.Ala136=
ENST00000428886.6:n.428G=
ENST00000436873.6:c.406G= ENSP00000398136.2:p.Ala136=
ENST00000528571.5:c.*146G= ENSP00000434647.1:n.*146G=
ENST00000530040.1:n.518G=
ENST00000533371.5:c.-324G= ENSP00000437066.1:n.-324G=
ENST00000534644.5:n.391G=
ENST00000611494.4:c.406G= ENSP00000484546.1:p.Ala136=
NM_000391.3:c.406G= NP_000382.3:p.Ala136=
NM_000391.4:c.406G= MANE Select NP_000382.3:p.Ala136=