Canonical Allele Identifier: CA1950215235
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617648G= , CM000673.2:g.6617648G= GRCh38
NC_000011.9:g.6638879G= , CM000673.1:g.6638879G= GRCh37
NC_000011.8:g.6595455G= NCBI36
NG_008653.1:g.6814C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.244C= ENSP00000507321.1:p.Leu82=
ENST00000299427.12:c.358C= MANE Select ENSP00000299427.6:p.Leu120=
ENST00000428886.7:n.446C=
ENST00000436873.7:c.162C=
ENST00000524788.2:n.1370C=
ENST00000524903.2:n.1486C=
ENST00000528571.6:c.*98C= ENSP00000434647.1:n.*98C=
ENST00000530040.2:n.387C=
ENST00000533371.6:c.-372C= ENSP00000437066.1:n.-372C=
ENST00000534644.6:n.359C=
ENST00000642892.1:c.-319C= ENSP00000494165.1:n.-319C=
ENST00000643439.1:c.*98C= ENSP00000495849.1:n.*98C=
ENST00000643479.1:n.387C=
ENST00000643516.1:c.245C=
ENST00000644151.1:n.1650C=
ENST00000644218.1:c.358C= ENSP00000493574.1:p.Leu120=
ENST00000644683.1:c.358C= ENSP00000494085.1:p.Leu120=
ENST00000644810.1:c.230-495C= ENSP00000495895.1:n.230-495C=
ENST00000644831.1:n.387C=
ENST00000644933.1:c.-372C= ENSP00000496133.1:n.-372C=
ENST00000645020.1:n.1386C=
ENST00000645285.1:c.-372C= ENSP00000495058.1:n.-372C=
ENST00000645331.1:n.380C=
ENST00000645620.1:c.-314C= ENSP00000493657.1:n.-314C=
ENST00000646777.1:n.387C=
ENST00000647016.1:n.691C=
ENST00000647152.1:c.-372C= ENSP00000495893.1:n.-372C=
ENST00000647209.1:c.*227C= ENSP00000495558.1:n.*227C=
ENST00000647346.1:n.1378C=
ENST00000299427.10:c.358C= ENSP00000299427.6:p.Leu120=
ENST00000428886.6:n.380C=
ENST00000436873.6:c.358C= ENSP00000398136.2:p.Leu120=
ENST00000528571.5:c.*98C= ENSP00000434647.1:n.*98C=
ENST00000530040.1:n.470C=
ENST00000533371.5:c.-372C= ENSP00000437066.1:n.-372C=
ENST00000534644.5:n.343C=
ENST00000611494.4:c.358C= ENSP00000484546.1:p.Leu120=
NM_000391.3:c.358C= NP_000382.3:p.Leu120=
NM_000391.4:c.358C= MANE Select NP_000382.3:p.Leu120=