Canonical Allele Identifier: CA1950237997
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617103C= , CM000673.2:g.6617103C= GRCh38
NC_000011.9:g.6638334C= , CM000673.1:g.6638334C= GRCh37
NC_000011.8:g.6594910C= NCBI36
NG_008653.1:g.7359G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.445G= ENSP00000507321.1:p.Glu149=
ENST00000299427.12:c.559G= MANE Select ENSP00000299427.6:p.Glu187=
ENST00000428886.7:n.794G=
ENST00000436873.7:c.312+198G=
ENST00000524788.2:n.1718G=
ENST00000524903.2:n.1834G=
ENST00000528807.2:n.215G=
ENST00000530040.2:n.479+256G=
ENST00000533371.6:c.-171G= ENSP00000437066.1:n.-171G=
ENST00000534644.6:n.507G=
ENST00000642892.1:c.-171G= ENSP00000494165.1:n.-171G=
ENST00000643439.1:c.*299G= ENSP00000495849.1:n.*299G=
ENST00000643479.1:n.588G=
ENST00000643516.1:c.395+198G=
ENST00000644151.1:n.1998G=
ENST00000644218.1:c.559G= ENSP00000493574.1:p.Glu187=
ENST00000644683.1:c.*12G= ENSP00000494085.1:n.*12G=
ENST00000644810.1:c.280G= ENSP00000495895.1:p.Glu94=
ENST00000644831.1:n.735G=
ENST00000644933.1:c.-171G= ENSP00000496133.1:n.-171G=
ENST00000645020.1:n.1734G=
ENST00000645285.1:c.-171G= ENSP00000495058.1:n.-171G=
ENST00000645331.1:n.925G=
ENST00000645620.1:c.-171G= ENSP00000493657.1:n.-171G=
ENST00000646777.1:n.735G=
ENST00000647016.1:n.1039G=
ENST00000647152.1:c.-171G= ENSP00000495893.1:n.-171G=
ENST00000647209.1:c.*428G= ENSP00000495558.1:n.*428G=
ENST00000647346.1:n.1579G=
ENST00000299427.10:c.559G= ENSP00000299427.6:p.Glu187=
ENST00000428886.6:n.728G=
ENST00000436873.6:c.450+256G= ENSP00000398136.2:n.450+256G=
ENST00000524788.1:n.259G=
ENST00000528571.5:c.*299G= ENSP00000434647.1:n.*299G=
ENST00000528807.1:n.109G=
ENST00000533371.5:c.-171G= ENSP00000437066.1:n.-171G=
ENST00000534644.5:n.544G=
ENST00000611494.4:c.559G= ENSP00000484546.1:p.Glu187=
NM_000391.3:c.559G= NP_000382.3:p.Glu187=
NM_000391.4:c.559G= MANE Select NP_000382.3:p.Glu187=