Canonical Allele Identifier: CA379476130
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617630T>A , CM000673.2:g.6617630T>A GRCh38
NC_000011.9:g.6638861T>A , CM000673.1:g.6638861T>A GRCh37
NC_000011.8:g.6595437T>A NCBI36
NG_008653.1:g.6832A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.262A>T ENSP00000507321.1:p.Ile88Phe
ENST00000299427.12:c.376A>T MANE Select ENSP00000299427.6:p.Ile126Phe
ENST00000428886.7:n.464A>T
ENST00000436873.7:c.180A>T
ENST00000524788.2:n.1388A>T
ENST00000524903.2:n.1504A>T
ENST00000528571.6:c.*116A>T ENSP00000434647.1:n.*116A>T
ENST00000530040.2:n.405A>T
ENST00000533371.6:c.-354A>T ENSP00000437066.1:n.-354A>T
ENST00000534644.6:n.377A>T
ENST00000642892.1:c.-301A>T ENSP00000494165.1:n.-301A>T
ENST00000643439.1:c.*116A>T ENSP00000495849.1:n.*116A>T
ENST00000643479.1:n.405A>T
ENST00000643516.1:c.263A>T
ENST00000644151.1:n.1668A>T
ENST00000644218.1:c.376A>T ENSP00000493574.1:p.Ile126Phe
ENST00000644683.1:c.376A>T ENSP00000494085.1:p.Ile126Phe
ENST00000644810.1:c.230-477A>T ENSP00000495895.1:n.230-477A>T
ENST00000644831.1:n.405A>T
ENST00000644933.1:c.-354A>T ENSP00000496133.1:n.-354A>T
ENST00000645020.1:n.1404A>T
ENST00000645285.1:c.-354A>T ENSP00000495058.1:n.-354A>T
ENST00000645331.1:n.398A>T
ENST00000645620.1:c.-296A>T ENSP00000493657.1:n.-296A>T
ENST00000646777.1:n.405A>T
ENST00000647016.1:n.709A>T
ENST00000647152.1:c.-354A>T ENSP00000495893.1:n.-354A>T
ENST00000647209.1:c.*245A>T ENSP00000495558.1:n.*245A>T
ENST00000647346.1:n.1396A>T
ENST00000299427.10:c.376A>T ENSP00000299427.6:p.Ile126Phe
ENST00000428886.6:n.398A>T
ENST00000436873.6:c.376A>T ENSP00000398136.2:p.Ile126Phe
ENST00000528571.5:c.*116A>T ENSP00000434647.1:n.*116A>T
ENST00000530040.1:n.488A>T
ENST00000533371.5:c.-354A>T ENSP00000437066.1:n.-354A>T
ENST00000534644.5:n.361A>T
ENST00000611494.4:c.376A>T ENSP00000484546.1:p.Ile126Phe
NM_000391.3:c.376A>T NP_000382.3:p.Ile126Phe
NM_000391.4:c.376A>T MANE Select NP_000382.3:p.Ile126Phe