Canonical Allele Identifier: CA1950238101
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617140G= , CM000673.2:g.6617140G= GRCh38
NC_000011.9:g.6638371G= , CM000673.1:g.6638371G= GRCh37
NC_000011.8:g.6594947G= NCBI36
NG_008653.1:g.7322C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.408C= ENSP00000507321.1:p.His136=
ENST00000299427.12:c.522C= MANE Select ENSP00000299427.6:p.His174=
ENST00000428886.7:n.757C=
ENST00000436873.7:c.312+161C=
ENST00000524788.2:n.1681C=
ENST00000524903.2:n.1797C=
ENST00000528807.2:n.178C=
ENST00000530040.2:n.479+219C=
ENST00000533371.6:c.-208C= ENSP00000437066.1:n.-208C=
ENST00000534644.6:n.470C=
ENST00000642892.1:c.-208C= ENSP00000494165.1:n.-208C=
ENST00000643439.1:c.*262C= ENSP00000495849.1:n.*262C=
ENST00000643479.1:n.551C=
ENST00000643516.1:c.395+161C=
ENST00000644151.1:n.1961C=
ENST00000644218.1:c.522C= ENSP00000493574.1:p.His174=
ENST00000644683.1:c.464C= ENSP00000494085.1:p.Thr155=
ENST00000644810.1:c.243C= ENSP00000495895.1:p.His81=
ENST00000644831.1:n.698C=
ENST00000644933.1:c.-208C= ENSP00000496133.1:n.-208C=
ENST00000645020.1:n.1697C=
ENST00000645285.1:c.-208C= ENSP00000495058.1:n.-208C=
ENST00000645331.1:n.888C=
ENST00000645620.1:c.-208C= ENSP00000493657.1:n.-208C=
ENST00000646777.1:n.698C=
ENST00000647016.1:n.1002C=
ENST00000647152.1:c.-208C= ENSP00000495893.1:n.-208C=
ENST00000647209.1:c.*391C= ENSP00000495558.1:n.*391C=
ENST00000647346.1:n.1542C=
ENST00000299427.10:c.522C= ENSP00000299427.6:p.His174=
ENST00000428886.6:n.691C=
ENST00000436873.6:c.450+219C= ENSP00000398136.2:n.450+219C=
ENST00000524788.1:n.222C=
ENST00000528571.5:c.*262C= ENSP00000434647.1:n.*262C=
ENST00000528807.1:n.72C=
ENST00000533371.5:c.-208C= ENSP00000437066.1:n.-208C=
ENST00000534644.5:n.507C=
ENST00000611494.4:c.522C= ENSP00000484546.1:p.His174=
NM_000391.3:c.522C= NP_000382.3:p.His174=
NM_000391.4:c.522C= MANE Select NP_000382.3:p.His174=