Canonical Allele Identifier: CA1950237811
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617028T= , CM000673.2:g.6617028T= GRCh38
NC_000011.9:g.6638259T= , CM000673.1:g.6638259T= GRCh37
NC_000011.8:g.6594835T= NCBI36
NG_008653.1:g.7434A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.520A= ENSP00000507321.1:p.Thr174=
ENST00000299427.12:c.634A= MANE Select ENSP00000299427.6:p.Thr212=
ENST00000436873.7:c.312+273A=
ENST00000524788.2:n.1793A=
ENST00000524903.2:n.1909A=
ENST00000528807.2:n.290A=
ENST00000530040.2:n.479+331A=
ENST00000533371.6:c.-96A= ENSP00000437066.1:n.-96A=
ENST00000534644.6:n.582A=
ENST00000642892.1:c.-96A= ENSP00000494165.1:n.-96A=
ENST00000643439.1:c.*374A= ENSP00000495849.1:n.*374A=
ENST00000643479.1:n.663A=
ENST00000643516.1:c.395+273A=
ENST00000644151.1:n.2073A=
ENST00000644218.1:c.634A= ENSP00000493574.1:p.Thr212=
ENST00000644683.1:c.*87A= ENSP00000494085.1:n.*87A=
ENST00000644810.1:c.355A= ENSP00000495895.1:p.Thr119=
ENST00000644831.1:n.810A=
ENST00000644933.1:c.-96A= ENSP00000496133.1:n.-96A=
ENST00000645020.1:n.1809A=
ENST00000645285.1:c.-96A= ENSP00000495058.1:n.-96A=
ENST00000645331.1:n.1000A=
ENST00000645620.1:c.-96A= ENSP00000493657.1:n.-96A=
ENST00000646777.1:n.810A=
ENST00000647016.1:n.1114A=
ENST00000647152.1:c.-96A= ENSP00000495893.1:n.-96A=
ENST00000647209.1:c.*503A= ENSP00000495558.1:n.*503A=
ENST00000647346.1:n.1654A=
ENST00000299427.10:c.634A= ENSP00000299427.6:p.Thr212=
ENST00000428886.6:n.803A=
ENST00000436873.6:c.450+331A= ENSP00000398136.2:n.450+331A=
ENST00000524788.1:n.334A=
ENST00000528571.5:c.*374A= ENSP00000434647.1:n.*374A=
ENST00000528807.1:n.184A=
ENST00000533371.5:c.-96A= ENSP00000437066.1:n.-96A=
ENST00000534644.5:n.619A=
ENST00000611494.4:c.634A= ENSP00000484546.1:p.Thr212=
NM_000391.3:c.634A= NP_000382.3:p.Thr212=
NM_000391.4:c.634A= MANE Select NP_000382.3:p.Thr212=