Canonical Allele Identifier: CA1950238077
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617132G= , CM000673.2:g.6617132G= GRCh38
NC_000011.9:g.6638363G= , CM000673.1:g.6638363G= GRCh37
NC_000011.8:g.6594939G= NCBI36
NG_008653.1:g.7330C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.416C= ENSP00000507321.1:p.Pro139=
ENST00000299427.12:c.530C= MANE Select ENSP00000299427.6:p.Pro177=
ENST00000428886.7:n.765C=
ENST00000436873.7:c.312+169C=
ENST00000524788.2:n.1689C=
ENST00000524903.2:n.1805C=
ENST00000528807.2:n.186C=
ENST00000530040.2:n.479+227C=
ENST00000533371.6:c.-200C= ENSP00000437066.1:n.-200C=
ENST00000534644.6:n.478C=
ENST00000642892.1:c.-200C= ENSP00000494165.1:n.-200C=
ENST00000643439.1:c.*270C= ENSP00000495849.1:n.*270C=
ENST00000643479.1:n.559C=
ENST00000643516.1:c.395+169C=
ENST00000644151.1:n.1969C=
ENST00000644218.1:c.530C= ENSP00000493574.1:p.Pro177=
ENST00000644683.1:c.472C= ENSP00000494085.1:p.Pro158=
ENST00000644810.1:c.251C= ENSP00000495895.1:p.Pro84=
ENST00000644831.1:n.706C=
ENST00000644933.1:c.-200C= ENSP00000496133.1:n.-200C=
ENST00000645020.1:n.1705C=
ENST00000645285.1:c.-200C= ENSP00000495058.1:n.-200C=
ENST00000645331.1:n.896C=
ENST00000645620.1:c.-200C= ENSP00000493657.1:n.-200C=
ENST00000646777.1:n.706C=
ENST00000647016.1:n.1010C=
ENST00000647152.1:c.-200C= ENSP00000495893.1:n.-200C=
ENST00000647209.1:c.*399C= ENSP00000495558.1:n.*399C=
ENST00000647346.1:n.1550C=
ENST00000299427.10:c.530C= ENSP00000299427.6:p.Pro177=
ENST00000428886.6:n.699C=
ENST00000436873.6:c.450+227C= ENSP00000398136.2:n.450+227C=
ENST00000524788.1:n.230C=
ENST00000528571.5:c.*270C= ENSP00000434647.1:n.*270C=
ENST00000528807.1:n.80C=
ENST00000533371.5:c.-200C= ENSP00000437066.1:n.-200C=
ENST00000534644.5:n.515C=
ENST00000611494.4:c.530C= ENSP00000484546.1:p.Pro177=
NM_000391.3:c.530C= NP_000382.3:p.Pro177=
NM_000391.4:c.530C= MANE Select NP_000382.3:p.Pro177=