Canonical Allele Identifier: CA1950214826
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617313G= , CM000673.2:g.6617313G= GRCh38
NC_000011.9:g.6638544G= , CM000673.1:g.6638544G= GRCh37
NC_000011.8:g.6595120G= NCBI36
NG_008653.1:g.7149C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.382C= ENSP00000507321.1:p.His128=
ENST00000299427.12:c.496C= MANE Select ENSP00000299427.6:p.His166=
ENST00000428886.7:n.584C=
ENST00000436873.7:c.300C=
ENST00000524788.2:n.1508C=
ENST00000524903.2:n.1624C=
ENST00000528571.6:c.*236C= ENSP00000434647.1:n.*236C=
ENST00000528807.2:n.152C=
ENST00000530040.2:n.479+46C=
ENST00000533371.6:c.-234C= ENSP00000437066.1:n.-234C=
ENST00000534644.6:n.456+41C=
ENST00000642892.1:c.-222+41C= ENSP00000494165.1:n.-222+41C=
ENST00000643439.1:c.*236C= ENSP00000495849.1:n.*236C=
ENST00000643479.1:n.525C=
ENST00000643516.1:c.383C=
ENST00000644151.1:n.1788C=
ENST00000644218.1:c.496C= ENSP00000493574.1:p.His166=
ENST00000644683.1:c.450+46C= ENSP00000494085.1:n.450+46C=
ENST00000644810.1:c.230-160C= ENSP00000495895.1:n.230-160C=
ENST00000644831.1:n.525C=
ENST00000644933.1:c.-234C= ENSP00000496133.1:n.-234C=
ENST00000645020.1:n.1524C=
ENST00000645285.1:c.-234C= ENSP00000495058.1:n.-234C=
ENST00000645331.1:n.715C=
ENST00000645620.1:c.-222+46C= ENSP00000493657.1:n.-222+46C=
ENST00000646777.1:n.525C=
ENST00000647016.1:n.829C=
ENST00000647152.1:c.-234C= ENSP00000495893.1:n.-234C=
ENST00000647209.1:c.*365C= ENSP00000495558.1:n.*365C=
ENST00000647346.1:n.1516C=
ENST00000299427.10:c.496C= ENSP00000299427.6:p.His166=
ENST00000428886.6:n.518C=
ENST00000436873.6:c.450+46C= ENSP00000398136.2:n.450+46C=
ENST00000524788.1:n.49C=
ENST00000528571.5:c.*236C= ENSP00000434647.1:n.*236C=
ENST00000533371.5:c.-234C= ENSP00000437066.1:n.-234C=
ENST00000534644.5:n.481C=
ENST00000611494.4:c.496C= ENSP00000484546.1:p.His166=
NM_000391.3:c.496C= NP_000382.3:p.His166=
NM_000391.4:c.496C= MANE Select NP_000382.3:p.His166=