Canonical Allele Identifier: CA1950238081
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617133G= , CM000673.2:g.6617133G= GRCh38
NC_000011.9:g.6638364G= , CM000673.1:g.6638364G= GRCh37
NC_000011.8:g.6594940G= NCBI36
NG_008653.1:g.7329C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.415C= ENSP00000507321.1:p.Pro139=
ENST00000299427.12:c.529C= MANE Select ENSP00000299427.6:p.Pro177=
ENST00000428886.7:n.764C=
ENST00000436873.7:c.312+168C=
ENST00000524788.2:n.1688C=
ENST00000524903.2:n.1804C=
ENST00000528807.2:n.185C=
ENST00000530040.2:n.479+226C=
ENST00000533371.6:c.-201C= ENSP00000437066.1:n.-201C=
ENST00000534644.6:n.477C=
ENST00000642892.1:c.-201C= ENSP00000494165.1:n.-201C=
ENST00000643439.1:c.*269C= ENSP00000495849.1:n.*269C=
ENST00000643479.1:n.558C=
ENST00000643516.1:c.395+168C=
ENST00000644151.1:n.1968C=
ENST00000644218.1:c.529C= ENSP00000493574.1:p.Pro177=
ENST00000644683.1:c.471C= ENSP00000494085.1:p.Phe157=
ENST00000644810.1:c.250C= ENSP00000495895.1:p.Pro84=
ENST00000644831.1:n.705C=
ENST00000644933.1:c.-201C= ENSP00000496133.1:n.-201C=
ENST00000645020.1:n.1704C=
ENST00000645285.1:c.-201C= ENSP00000495058.1:n.-201C=
ENST00000645331.1:n.895C=
ENST00000645620.1:c.-201C= ENSP00000493657.1:n.-201C=
ENST00000646777.1:n.705C=
ENST00000647016.1:n.1009C=
ENST00000647152.1:c.-201C= ENSP00000495893.1:n.-201C=
ENST00000647209.1:c.*398C= ENSP00000495558.1:n.*398C=
ENST00000647346.1:n.1549C=
ENST00000299427.10:c.529C= ENSP00000299427.6:p.Pro177=
ENST00000428886.6:n.698C=
ENST00000436873.6:c.450+226C= ENSP00000398136.2:n.450+226C=
ENST00000524788.1:n.229C=
ENST00000528571.5:c.*269C= ENSP00000434647.1:n.*269C=
ENST00000528807.1:n.79C=
ENST00000533371.5:c.-201C= ENSP00000437066.1:n.-201C=
ENST00000534644.5:n.514C=
ENST00000611494.4:c.529C= ENSP00000484546.1:p.Pro177=
NM_000391.3:c.529C= NP_000382.3:p.Pro177=
NM_000391.4:c.529C= MANE Select NP_000382.3:p.Pro177=