Canonical Allele Identifier: CA1950214947
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617393T= , CM000673.2:g.6617393T= GRCh38
NC_000011.9:g.6638624T= , CM000673.1:g.6638624T= GRCh37
NC_000011.8:g.6595200T= NCBI36
NG_008653.1:g.7069A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.302A= ENSP00000507321.1:p.His101=
ENST00000299427.12:c.416A= MANE Select ENSP00000299427.6:p.His139=
ENST00000428886.7:n.504A=
ENST00000436873.7:c.220A=
ENST00000524788.2:n.1428A=
ENST00000524903.2:n.1544A=
ENST00000528571.6:c.*156A= ENSP00000434647.1:n.*156A=
ENST00000528807.2:n.72A=
ENST00000530040.2:n.445A=
ENST00000533371.6:c.-314A= ENSP00000437066.1:n.-314A=
ENST00000534644.6:n.417A=
ENST00000642892.1:c.-261A= ENSP00000494165.1:n.-261A=
ENST00000643439.1:c.*156A= ENSP00000495849.1:n.*156A=
ENST00000643479.1:n.445A=
ENST00000643516.1:c.303A=
ENST00000644151.1:n.1708A=
ENST00000644218.1:c.416A= ENSP00000493574.1:p.His139=
ENST00000644683.1:c.416A= ENSP00000494085.1:p.His139=
ENST00000644810.1:c.230-240A= ENSP00000495895.1:n.230-240A=
ENST00000644831.1:n.445A=
ENST00000644933.1:c.-314A= ENSP00000496133.1:n.-314A=
ENST00000645020.1:n.1444A=
ENST00000645285.1:c.-314A= ENSP00000495058.1:n.-314A=
ENST00000645331.1:n.635A=
ENST00000645620.1:c.-256A= ENSP00000493657.1:n.-256A=
ENST00000646777.1:n.445A=
ENST00000647016.1:n.749A=
ENST00000647152.1:c.-314A= ENSP00000495893.1:n.-314A=
ENST00000647209.1:c.*285A= ENSP00000495558.1:n.*285A=
ENST00000647346.1:n.1436A=
ENST00000299427.10:c.416A= ENSP00000299427.6:p.His139=
ENST00000428886.6:n.438A=
ENST00000436873.6:c.416A= ENSP00000398136.2:p.His139=
ENST00000528571.5:c.*156A= ENSP00000434647.1:n.*156A=
ENST00000530040.1:n.528A=
ENST00000533371.5:c.-314A= ENSP00000437066.1:n.-314A=
ENST00000534644.5:n.401A=
ENST00000611494.4:c.416A= ENSP00000484546.1:p.His139=
NM_000391.3:c.416A= NP_000382.3:p.His139=
NM_000391.4:c.416A= MANE Select NP_000382.3:p.His139=