Canonical Allele Identifier: CA1950214925
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617376G= , CM000673.2:g.6617376G= GRCh38
NC_000011.9:g.6638607G= , CM000673.1:g.6638607G= GRCh37
NC_000011.8:g.6595183G= NCBI36
NG_008653.1:g.7086C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.319C= ENSP00000507321.1:p.Pro107=
ENST00000299427.12:c.433C= MANE Select ENSP00000299427.6:p.Pro145=
ENST00000428886.7:n.521C=
ENST00000436873.7:c.237C=
ENST00000524788.2:n.1445C=
ENST00000524903.2:n.1561C=
ENST00000528571.6:c.*173C= ENSP00000434647.1:n.*173C=
ENST00000528807.2:n.89C=
ENST00000530040.2:n.462C=
ENST00000533371.6:c.-297C= ENSP00000437066.1:n.-297C=
ENST00000534644.6:n.434C=
ENST00000642892.1:c.-244C= ENSP00000494165.1:n.-244C=
ENST00000643439.1:c.*173C= ENSP00000495849.1:n.*173C=
ENST00000643479.1:n.462C=
ENST00000643516.1:c.320C=
ENST00000644151.1:n.1725C=
ENST00000644218.1:c.433C= ENSP00000493574.1:p.Pro145=
ENST00000644683.1:c.433C= ENSP00000494085.1:p.Pro145=
ENST00000644810.1:c.230-223C= ENSP00000495895.1:n.230-223C=
ENST00000644831.1:n.462C=
ENST00000644933.1:c.-297C= ENSP00000496133.1:n.-297C=
ENST00000645020.1:n.1461C=
ENST00000645285.1:c.-297C= ENSP00000495058.1:n.-297C=
ENST00000645331.1:n.652C=
ENST00000645620.1:c.-239C= ENSP00000493657.1:n.-239C=
ENST00000646777.1:n.462C=
ENST00000647016.1:n.766C=
ENST00000647152.1:c.-297C= ENSP00000495893.1:n.-297C=
ENST00000647209.1:c.*302C= ENSP00000495558.1:n.*302C=
ENST00000647346.1:n.1453C=
ENST00000299427.10:c.433C= ENSP00000299427.6:p.Pro145=
ENST00000428886.6:n.455C=
ENST00000436873.6:c.433C= ENSP00000398136.2:p.Pro145=
ENST00000528571.5:c.*173C= ENSP00000434647.1:n.*173C=
ENST00000530040.1:n.545C=
ENST00000533371.5:c.-297C= ENSP00000437066.1:n.-297C=
ENST00000534644.5:n.418C=
ENST00000611494.4:c.433C= ENSP00000484546.1:p.Pro145=
NM_000391.3:c.433C= NP_000382.3:p.Pro145=
NM_000391.4:c.433C= MANE Select NP_000382.3:p.Pro145=