Canonical Allele Identifier: CA379476538
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617737C>A , CM000673.2:g.6617737C>A GRCh38
NC_000011.9:g.6638968C>A , CM000673.1:g.6638968C>A GRCh37
NC_000011.8:g.6595544C>A NCBI36
NG_008653.1:g.6725G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.155G>T ENSP00000507321.1:p.Arg52Met
ENST00000299427.12:c.269G>T MANE Select ENSP00000299427.6:p.Arg90Met
ENST00000428886.7:n.357G>T
ENST00000436873.7:c.73G>T
ENST00000524788.2:n.1281G>T
ENST00000524903.2:n.1397G>T
ENST00000528571.6:c.*9G>T ENSP00000434647.1:n.*9G>T
ENST00000530040.2:n.298G>T
ENST00000533371.6:c.-461G>T ENSP00000437066.1:n.-461G>T
ENST00000534644.6:n.270G>T
ENST00000642892.1:c.-408G>T ENSP00000494165.1:n.-408G>T
ENST00000643439.1:c.*9G>T ENSP00000495849.1:n.*9G>T
ENST00000643479.1:n.298G>T
ENST00000643516.1:c.156G>T
ENST00000644151.1:n.1561G>T
ENST00000644218.1:c.269G>T ENSP00000493574.1:p.Arg90Met
ENST00000644683.1:c.269G>T ENSP00000494085.1:p.Arg90Met
ENST00000644810.1:c.230-584G>T ENSP00000495895.1:n.230-584G>T
ENST00000644831.1:n.298G>T
ENST00000644933.1:c.-461G>T ENSP00000496133.1:n.-461G>T
ENST00000645020.1:n.1297G>T
ENST00000645285.1:c.-461G>T ENSP00000495058.1:n.-461G>T
ENST00000645331.1:n.291G>T
ENST00000645620.1:c.-403G>T ENSP00000493657.1:n.-403G>T
ENST00000646777.1:n.298G>T
ENST00000647016.1:n.602G>T
ENST00000647152.1:c.-461G>T ENSP00000495893.1:n.-461G>T
ENST00000647209.1:c.*138G>T ENSP00000495558.1:n.*138G>T
ENST00000647346.1:n.1289G>T
ENST00000299427.10:c.269G>T ENSP00000299427.6:p.Arg90Met
ENST00000428886.6:n.291G>T
ENST00000436873.6:c.269G>T ENSP00000398136.2:p.Arg90Met
ENST00000528571.5:c.*9G>T ENSP00000434647.1:n.*9G>T
ENST00000530040.1:n.381G>T
ENST00000533371.5:c.-461G>T ENSP00000437066.1:n.-461G>T
ENST00000534644.5:n.254G>T
ENST00000611494.4:c.269G>T ENSP00000484546.1:p.Arg90Met
NM_000391.3:c.269G>T NP_000382.3:p.Arg90Met
NM_000391.4:c.269G>T MANE Select NP_000382.3:p.Arg90Met