Canonical Allele Identifier: CA1950214917
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617373T= , CM000673.2:g.6617373T= GRCh38
NC_000011.9:g.6638604T= , CM000673.1:g.6638604T= GRCh37
NC_000011.8:g.6595180T= NCBI36
NG_008653.1:g.7089A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.322A= ENSP00000507321.1:p.Thr108=
ENST00000299427.12:c.436A= MANE Select ENSP00000299427.6:p.Thr146=
ENST00000428886.7:n.524A=
ENST00000436873.7:c.240A=
ENST00000524788.2:n.1448A=
ENST00000524903.2:n.1564A=
ENST00000528571.6:c.*176A= ENSP00000434647.1:n.*176A=
ENST00000528807.2:n.92A=
ENST00000530040.2:n.465A=
ENST00000533371.6:c.-294A= ENSP00000437066.1:n.-294A=
ENST00000534644.6:n.437A=
ENST00000642892.1:c.-241A= ENSP00000494165.1:n.-241A=
ENST00000643439.1:c.*176A= ENSP00000495849.1:n.*176A=
ENST00000643479.1:n.465A=
ENST00000643516.1:c.323A=
ENST00000644151.1:n.1728A=
ENST00000644218.1:c.436A= ENSP00000493574.1:p.Thr146=
ENST00000644683.1:c.436A= ENSP00000494085.1:p.Thr146=
ENST00000644810.1:c.230-220A= ENSP00000495895.1:n.230-220A=
ENST00000644831.1:n.465A=
ENST00000644933.1:c.-294A= ENSP00000496133.1:n.-294A=
ENST00000645020.1:n.1464A=
ENST00000645285.1:c.-294A= ENSP00000495058.1:n.-294A=
ENST00000645331.1:n.655A=
ENST00000645620.1:c.-236A= ENSP00000493657.1:n.-236A=
ENST00000646777.1:n.465A=
ENST00000647016.1:n.769A=
ENST00000647152.1:c.-294A= ENSP00000495893.1:n.-294A=
ENST00000647209.1:c.*305A= ENSP00000495558.1:n.*305A=
ENST00000647346.1:n.1456A=
ENST00000299427.10:c.436A= ENSP00000299427.6:p.Thr146=
ENST00000428886.6:n.458A=
ENST00000436873.6:c.436A= ENSP00000398136.2:p.Thr146=
ENST00000528571.5:c.*176A= ENSP00000434647.1:n.*176A=
ENST00000530040.1:n.548A=
ENST00000533371.5:c.-294A= ENSP00000437066.1:n.-294A=
ENST00000534644.5:n.421A=
ENST00000611494.4:c.436A= ENSP00000484546.1:p.Thr146=
NM_000391.3:c.436A= NP_000382.3:p.Thr146=
NM_000391.4:c.436A= MANE Select NP_000382.3:p.Thr146=