Canonical Allele Identifier: CA1950237886
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617054G= , CM000673.2:g.6617054G= GRCh38
NC_000011.9:g.6638285G= , CM000673.1:g.6638285G= GRCh37
NC_000011.8:g.6594861G= NCBI36
NG_008653.1:g.7408C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.494C= ENSP00000507321.1:p.Ser165=
ENST00000299427.12:c.608C= MANE Select ENSP00000299427.6:p.Ser203=
ENST00000436873.7:c.312+247C=
ENST00000524788.2:n.1767C=
ENST00000524903.2:n.1883C=
ENST00000528807.2:n.264C=
ENST00000530040.2:n.479+305C=
ENST00000533371.6:c.-122C= ENSP00000437066.1:n.-122C=
ENST00000534644.6:n.556C=
ENST00000642892.1:c.-122C= ENSP00000494165.1:n.-122C=
ENST00000643439.1:c.*348C= ENSP00000495849.1:n.*348C=
ENST00000643479.1:n.637C=
ENST00000643516.1:c.395+247C=
ENST00000644151.1:n.2047C=
ENST00000644218.1:c.608C= ENSP00000493574.1:p.Ser203=
ENST00000644683.1:c.*61C= ENSP00000494085.1:n.*61C=
ENST00000644810.1:c.329C= ENSP00000495895.1:p.Ser110=
ENST00000644831.1:n.784C=
ENST00000644933.1:c.-122C= ENSP00000496133.1:n.-122C=
ENST00000645020.1:n.1783C=
ENST00000645285.1:c.-122C= ENSP00000495058.1:n.-122C=
ENST00000645331.1:n.974C=
ENST00000645620.1:c.-122C= ENSP00000493657.1:n.-122C=
ENST00000646777.1:n.784C=
ENST00000647016.1:n.1088C=
ENST00000647152.1:c.-122C= ENSP00000495893.1:n.-122C=
ENST00000647209.1:c.*477C= ENSP00000495558.1:n.*477C=
ENST00000647346.1:n.1628C=
ENST00000299427.10:c.608C= ENSP00000299427.6:p.Ser203=
ENST00000428886.6:n.777C=
ENST00000436873.6:c.450+305C= ENSP00000398136.2:n.450+305C=
ENST00000524788.1:n.308C=
ENST00000528571.5:c.*348C= ENSP00000434647.1:n.*348C=
ENST00000528807.1:n.158C=
ENST00000533371.5:c.-122C= ENSP00000437066.1:n.-122C=
ENST00000534644.5:n.593C=
ENST00000611494.4:c.608C= ENSP00000484546.1:p.Ser203=
NM_000391.3:c.608C= NP_000382.3:p.Ser203=
NM_000391.4:c.608C= MANE Select NP_000382.3:p.Ser203=