Canonical Allele Identifier: CA379476436
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617707T>A , CM000673.2:g.6617707T>A GRCh38
NC_000011.9:g.6638938T>A , CM000673.1:g.6638938T>A GRCh37
NC_000011.8:g.6595514T>A NCBI36
NG_008653.1:g.6755A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.185A>T ENSP00000507321.1:p.Gln62Leu
ENST00000299427.12:c.299A>T MANE Select ENSP00000299427.6:p.Gln100Leu
ENST00000428886.7:n.387A>T
ENST00000436873.7:c.103A>T
ENST00000524788.2:n.1311A>T
ENST00000524903.2:n.1427A>T
ENST00000528571.6:c.*39A>T ENSP00000434647.1:n.*39A>T
ENST00000530040.2:n.328A>T
ENST00000533371.6:c.-431A>T ENSP00000437066.1:n.-431A>T
ENST00000534644.6:n.300A>T
ENST00000642892.1:c.-378A>T ENSP00000494165.1:n.-378A>T
ENST00000643439.1:c.*39A>T ENSP00000495849.1:n.*39A>T
ENST00000643479.1:n.328A>T
ENST00000643516.1:c.186A>T
ENST00000644151.1:n.1591A>T
ENST00000644218.1:c.299A>T ENSP00000493574.1:p.Gln100Leu
ENST00000644683.1:c.299A>T ENSP00000494085.1:p.Gln100Leu
ENST00000644810.1:c.230-554A>T ENSP00000495895.1:n.230-554A>T
ENST00000644831.1:n.328A>T
ENST00000644933.1:c.-431A>T ENSP00000496133.1:n.-431A>T
ENST00000645020.1:n.1327A>T
ENST00000645285.1:c.-431A>T ENSP00000495058.1:n.-431A>T
ENST00000645331.1:n.321A>T
ENST00000645620.1:c.-373A>T ENSP00000493657.1:n.-373A>T
ENST00000646777.1:n.328A>T
ENST00000647016.1:n.632A>T
ENST00000647152.1:c.-431A>T ENSP00000495893.1:n.-431A>T
ENST00000647209.1:c.*168A>T ENSP00000495558.1:n.*168A>T
ENST00000647346.1:n.1319A>T
ENST00000299427.10:c.299A>T ENSP00000299427.6:p.Gln100Leu
ENST00000428886.6:n.321A>T
ENST00000436873.6:c.299A>T ENSP00000398136.2:p.Gln100Leu
ENST00000528571.5:c.*39A>T ENSP00000434647.1:n.*39A>T
ENST00000530040.1:n.411A>T
ENST00000533371.5:c.-431A>T ENSP00000437066.1:n.-431A>T
ENST00000534644.5:n.284A>T
ENST00000611494.4:c.299A>T ENSP00000484546.1:p.Gln100Leu
NM_000391.3:c.299A>T NP_000382.3:p.Gln100Leu
NM_000391.4:c.299A>T MANE Select NP_000382.3:p.Gln100Leu