Canonical Allele Identifier: CA1950215559
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6618010C= , CM000673.2:g.6618010C= GRCh38
NC_000011.9:g.6639241C= , CM000673.1:g.6639241C= GRCh37
NC_000011.8:g.6595817C= NCBI36
NG_008653.1:g.6452G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-234G= ENSP00000507321.1:n.116-234G=
ENST00000299427.12:c.230-234G= MANE Select ENSP00000299427.6:n.230-234G=
ENST00000428886.7:n.318-234G=
ENST00000436873.7:c.34-234G=
ENST00000524788.2:n.1008G=
ENST00000524903.2:n.1124G=
ENST00000528571.6:c.90-234G= ENSP00000434647.1:n.90-234G=
ENST00000530040.2:n.259-234G=
ENST00000533371.6:c.-500-234G= ENSP00000437066.1:n.-500-234G=
ENST00000534644.6:n.231-234G=
ENST00000642892.1:c.-447-234G= ENSP00000494165.1:n.-447-234G=
ENST00000643439.1:c.90-234G= ENSP00000495849.1:n.90-234G=
ENST00000643479.1:n.259-234G=
ENST00000643516.1:c.117-234G=
ENST00000644151.1:n.1288G=
ENST00000644218.1:c.230-234G= ENSP00000493574.1:n.230-234G=
ENST00000644683.1:c.230-234G= ENSP00000494085.1:n.230-234G=
ENST00000644810.1:c.229+766G= ENSP00000495895.1:n.229+766G=
ENST00000644831.1:n.259-234G=
ENST00000644933.1:c.-500-234G= ENSP00000496133.1:n.-500-234G=
ENST00000645020.1:n.1024G=
ENST00000645285.1:c.-500-234G= ENSP00000495058.1:n.-500-234G=
ENST00000645331.1:n.252-234G=
ENST00000645620.1:c.-442-234G= ENSP00000493657.1:n.-442-234G=
ENST00000646777.1:n.259-234G=
ENST00000647016.1:n.329G=
ENST00000647152.1:c.-500-234G= ENSP00000495893.1:n.-500-234G=
ENST00000647209.1:c.*99-234G= ENSP00000495558.1:n.*99-234G=
ENST00000647346.1:n.1016G=
ENST00000299427.10:c.230-234G= ENSP00000299427.6:n.230-234G=
ENST00000428886.6:n.252-234G=
ENST00000436873.6:c.230-234G= ENSP00000398136.2:n.230-234G=
ENST00000528571.5:c.90-234G= ENSP00000434647.1:n.90-234G=
ENST00000528917.1:n.531-234G=
ENST00000530040.1:n.342-234G=
ENST00000533371.5:c.-500-234G= ENSP00000437066.1:n.-500-234G=
ENST00000534644.5:n.215-234G=
ENST00000611494.4:c.230-234G= ENSP00000484546.1:n.230-234G=
NM_000391.3:c.230-234G= NP_000382.3:n.230-234G=
NM_000391.4:c.230-234G= MANE Select NP_000382.3:n.230-234G=