Canonical Allele Identifier: CA1950237930
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617072T= , CM000673.2:g.6617072T= GRCh38
NC_000011.9:g.6638303T= , CM000673.1:g.6638303T= GRCh37
NC_000011.8:g.6594879T= NCBI36
NG_008653.1:g.7390A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.476A= ENSP00000507321.1:p.His159=
ENST00000299427.12:c.590A= MANE Select ENSP00000299427.6:p.His197=
ENST00000428886.7:n.825A=
ENST00000436873.7:c.312+229A=
ENST00000524788.2:n.1749A=
ENST00000524903.2:n.1865A=
ENST00000528807.2:n.246A=
ENST00000530040.2:n.479+287A=
ENST00000533371.6:c.-140A= ENSP00000437066.1:n.-140A=
ENST00000534644.6:n.538A=
ENST00000642892.1:c.-140A= ENSP00000494165.1:n.-140A=
ENST00000643439.1:c.*330A= ENSP00000495849.1:n.*330A=
ENST00000643479.1:n.619A=
ENST00000643516.1:c.395+229A=
ENST00000644151.1:n.2029A=
ENST00000644218.1:c.590A= ENSP00000493574.1:p.His197=
ENST00000644683.1:c.*43A= ENSP00000494085.1:n.*43A=
ENST00000644810.1:c.311A= ENSP00000495895.1:p.His104=
ENST00000644831.1:n.766A=
ENST00000644933.1:c.-140A= ENSP00000496133.1:n.-140A=
ENST00000645020.1:n.1765A=
ENST00000645285.1:c.-140A= ENSP00000495058.1:n.-140A=
ENST00000645331.1:n.956A=
ENST00000645620.1:c.-140A= ENSP00000493657.1:n.-140A=
ENST00000646777.1:n.766A=
ENST00000647016.1:n.1070A=
ENST00000647152.1:c.-140A= ENSP00000495893.1:n.-140A=
ENST00000647209.1:c.*459A= ENSP00000495558.1:n.*459A=
ENST00000647346.1:n.1610A=
ENST00000299427.10:c.590A= ENSP00000299427.6:p.His197=
ENST00000428886.6:n.759A=
ENST00000436873.6:c.450+287A= ENSP00000398136.2:n.450+287A=
ENST00000524788.1:n.290A=
ENST00000528571.5:c.*330A= ENSP00000434647.1:n.*330A=
ENST00000528807.1:n.140A=
ENST00000533371.5:c.-140A= ENSP00000437066.1:n.-140A=
ENST00000534644.5:n.575A=
ENST00000611494.4:c.590A= ENSP00000484546.1:p.His197=
NM_000391.3:c.590A= NP_000382.3:p.His197=
NM_000391.4:c.590A= MANE Select NP_000382.3:p.His197=