Canonical Allele Identifier: CA1950238331
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617254C= , CM000673.2:g.6617254C= GRCh38
NC_000011.9:g.6638485C= , CM000673.1:g.6638485C= GRCh37
NC_000011.8:g.6595061C= NCBI36
NG_008653.1:g.7208G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.394+47G= ENSP00000507321.1:n.394+47G=
ENST00000299427.12:c.508+47G= MANE Select ENSP00000299427.6:n.508+47G=
ENST00000428886.7:n.643G=
ENST00000436873.7:c.312+47G=
ENST00000524788.2:n.1567G=
ENST00000524903.2:n.1683G=
ENST00000528571.6:c.*295G= ENSP00000434647.1:n.*295G=
ENST00000528807.2:n.164+47G=
ENST00000530040.2:n.479+105G=
ENST00000533371.6:c.-222+47G= ENSP00000437066.1:n.-222+47G=
ENST00000534644.6:n.457-101G=
ENST00000642892.1:c.-221-101G= ENSP00000494165.1:n.-221-101G=
ENST00000643439.1:c.*248+47G= ENSP00000495849.1:n.*248+47G=
ENST00000643479.1:n.537+47G=
ENST00000643516.1:c.395+47G=
ENST00000644151.1:n.1847G=
ENST00000644218.1:c.508+47G= ENSP00000493574.1:n.508+47G=
ENST00000644683.1:c.451-101G= ENSP00000494085.1:n.451-101G=
ENST00000644810.1:c.230-101G= ENSP00000495895.1:n.230-101G=
ENST00000644831.1:n.584G=
ENST00000644933.1:c.-222+47G= ENSP00000496133.1:n.-222+47G=
ENST00000645020.1:n.1583G=
ENST00000645285.1:c.-222+47G= ENSP00000495058.1:n.-222+47G=
ENST00000645331.1:n.774G=
ENST00000645620.1:c.-221-101G= ENSP00000493657.1:n.-221-101G=
ENST00000646777.1:n.584G=
ENST00000647016.1:n.888G=
ENST00000647152.1:c.-222+47G= ENSP00000495893.1:n.-222+47G=
ENST00000647209.1:c.*377+47G= ENSP00000495558.1:n.*377+47G=
ENST00000647346.1:n.1528+47G=
ENST00000299427.10:c.508+47G= ENSP00000299427.6:n.508+47G=
ENST00000428886.6:n.577G=
ENST00000436873.6:c.450+105G= ENSP00000398136.2:n.450+105G=
ENST00000524788.1:n.108G=
ENST00000528571.5:c.*248+47G= ENSP00000434647.1:n.*248+47G=
ENST00000533371.5:c.-222+47G= ENSP00000437066.1:n.-222+47G=
ENST00000534644.5:n.493+47G=
ENST00000611494.4:c.508+47G= ENSP00000484546.1:n.508+47G=
NM_000391.3:c.508+47G= NP_000382.3:n.508+47G=
NM_000391.4:c.508+47G= MANE Select NP_000382.3:n.508+47G=