Canonical Allele Identifier: CA1950237906
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617059G= , CM000673.2:g.6617059G= GRCh38
NC_000011.9:g.6638290G= , CM000673.1:g.6638290G= GRCh37
NC_000011.8:g.6594866G= NCBI36
NG_008653.1:g.7403C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.489C= ENSP00000507321.1:p.Thr163=
ENST00000299427.12:c.603C= MANE Select ENSP00000299427.6:p.Thr201=
ENST00000436873.7:c.312+242C=
ENST00000524788.2:n.1762C=
ENST00000524903.2:n.1878C=
ENST00000528807.2:n.259C=
ENST00000530040.2:n.479+300C=
ENST00000533371.6:c.-127C= ENSP00000437066.1:n.-127C=
ENST00000534644.6:n.551C=
ENST00000642892.1:c.-127C= ENSP00000494165.1:n.-127C=
ENST00000643439.1:c.*343C= ENSP00000495849.1:n.*343C=
ENST00000643479.1:n.632C=
ENST00000643516.1:c.395+242C=
ENST00000644151.1:n.2042C=
ENST00000644218.1:c.603C= ENSP00000493574.1:p.Thr201=
ENST00000644683.1:c.*56C= ENSP00000494085.1:n.*56C=
ENST00000644810.1:c.324C= ENSP00000495895.1:p.Thr108=
ENST00000644831.1:n.779C=
ENST00000644933.1:c.-127C= ENSP00000496133.1:n.-127C=
ENST00000645020.1:n.1778C=
ENST00000645285.1:c.-127C= ENSP00000495058.1:n.-127C=
ENST00000645331.1:n.969C=
ENST00000645620.1:c.-127C= ENSP00000493657.1:n.-127C=
ENST00000646777.1:n.779C=
ENST00000647016.1:n.1083C=
ENST00000647152.1:c.-127C= ENSP00000495893.1:n.-127C=
ENST00000647209.1:c.*472C= ENSP00000495558.1:n.*472C=
ENST00000647346.1:n.1623C=
ENST00000299427.10:c.603C= ENSP00000299427.6:p.Thr201=
ENST00000428886.6:n.772C=
ENST00000436873.6:c.450+300C= ENSP00000398136.2:n.450+300C=
ENST00000524788.1:n.303C=
ENST00000528571.5:c.*343C= ENSP00000434647.1:n.*343C=
ENST00000528807.1:n.153C=
ENST00000533371.5:c.-127C= ENSP00000437066.1:n.-127C=
ENST00000534644.5:n.588C=
ENST00000611494.4:c.603C= ENSP00000484546.1:p.Thr201=
NM_000391.3:c.603C= NP_000382.3:p.Thr201=
NM_000391.4:c.603C= MANE Select NP_000382.3:p.Thr201=