Canonical Allele Identifier: CA1950237855
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617045C= , CM000673.2:g.6617045C= GRCh38
NC_000011.9:g.6638276C= , CM000673.1:g.6638276C= GRCh37
NC_000011.8:g.6594852C= NCBI36
NG_008653.1:g.7417G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.503G= ENSP00000507321.1:p.Arg168=
ENST00000299427.12:c.617G= MANE Select ENSP00000299427.6:p.Arg206=
ENST00000436873.7:c.312+256G=
ENST00000524788.2:n.1776G=
ENST00000524903.2:n.1892G=
ENST00000528807.2:n.273G=
ENST00000530040.2:n.479+314G=
ENST00000533371.6:c.-113G= ENSP00000437066.1:n.-113G=
ENST00000534644.6:n.565G=
ENST00000642892.1:c.-113G= ENSP00000494165.1:n.-113G=
ENST00000643439.1:c.*357G= ENSP00000495849.1:n.*357G=
ENST00000643479.1:n.646G=
ENST00000643516.1:c.395+256G=
ENST00000644151.1:n.2056G=
ENST00000644218.1:c.617G= ENSP00000493574.1:p.Arg206=
ENST00000644683.1:c.*70G= ENSP00000494085.1:n.*70G=
ENST00000644810.1:c.338G= ENSP00000495895.1:p.Arg113=
ENST00000644831.1:n.793G=
ENST00000644933.1:c.-113G= ENSP00000496133.1:n.-113G=
ENST00000645020.1:n.1792G=
ENST00000645285.1:c.-113G= ENSP00000495058.1:n.-113G=
ENST00000645331.1:n.983G=
ENST00000645620.1:c.-113G= ENSP00000493657.1:n.-113G=
ENST00000646777.1:n.793G=
ENST00000647016.1:n.1097G=
ENST00000647152.1:c.-113G= ENSP00000495893.1:n.-113G=
ENST00000647209.1:c.*486G= ENSP00000495558.1:n.*486G=
ENST00000647346.1:n.1637G=
ENST00000299427.10:c.617G= ENSP00000299427.6:p.Arg206=
ENST00000428886.6:n.786G=
ENST00000436873.6:c.450+314G= ENSP00000398136.2:n.450+314G=
ENST00000524788.1:n.317G=
ENST00000528571.5:c.*357G= ENSP00000434647.1:n.*357G=
ENST00000528807.1:n.167G=
ENST00000533371.5:c.-113G= ENSP00000437066.1:n.-113G=
ENST00000534644.5:n.602G=
ENST00000611494.4:c.617G= ENSP00000484546.1:p.Arg206=
NM_000391.3:c.617G= NP_000382.3:p.Arg206=
NM_000391.4:c.617G= MANE Select NP_000382.3:p.Arg206=