Canonical Allele Identifier: CA1950214856
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617335C= , CM000673.2:g.6617335C= GRCh38
NC_000011.9:g.6638566C= , CM000673.1:g.6638566C= GRCh37
NC_000011.8:g.6595142C= NCBI36
NG_008653.1:g.7127G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.360G= ENSP00000507321.1:p.Gln120=
ENST00000299427.12:c.474G= MANE Select ENSP00000299427.6:p.Gln158=
ENST00000428886.7:n.562G=
ENST00000436873.7:c.278G=
ENST00000524788.2:n.1486G=
ENST00000524903.2:n.1602G=
ENST00000528571.6:c.*214G= ENSP00000434647.1:n.*214G=
ENST00000528807.2:n.130G=
ENST00000530040.2:n.479+24G=
ENST00000533371.6:c.-256G= ENSP00000437066.1:n.-256G=
ENST00000534644.6:n.456+19G=
ENST00000642892.1:c.-222+19G= ENSP00000494165.1:n.-222+19G=
ENST00000643439.1:c.*214G= ENSP00000495849.1:n.*214G=
ENST00000643479.1:n.503G=
ENST00000643516.1:c.361G=
ENST00000644151.1:n.1766G=
ENST00000644218.1:c.474G= ENSP00000493574.1:p.Gln158=
ENST00000644683.1:c.450+24G= ENSP00000494085.1:n.450+24G=
ENST00000644810.1:c.230-182G= ENSP00000495895.1:n.230-182G=
ENST00000644831.1:n.503G=
ENST00000644933.1:c.-256G= ENSP00000496133.1:n.-256G=
ENST00000645020.1:n.1502G=
ENST00000645285.1:c.-256G= ENSP00000495058.1:n.-256G=
ENST00000645331.1:n.693G=
ENST00000645620.1:c.-222+24G= ENSP00000493657.1:n.-222+24G=
ENST00000646777.1:n.503G=
ENST00000647016.1:n.807G=
ENST00000647152.1:c.-256G= ENSP00000495893.1:n.-256G=
ENST00000647209.1:c.*343G= ENSP00000495558.1:n.*343G=
ENST00000647346.1:n.1494G=
ENST00000299427.10:c.474G= ENSP00000299427.6:p.Gln158=
ENST00000428886.6:n.496G=
ENST00000436873.6:c.450+24G= ENSP00000398136.2:n.450+24G=
ENST00000524788.1:n.27G=
ENST00000528571.5:c.*214G= ENSP00000434647.1:n.*214G=
ENST00000533371.5:c.-256G= ENSP00000437066.1:n.-256G=
ENST00000534644.5:n.459G=
ENST00000611494.4:c.474G= ENSP00000484546.1:p.Gln158=
NM_000391.3:c.474G= NP_000382.3:p.Gln158=
NM_000391.4:c.474G= MANE Select NP_000382.3:p.Gln158=