Canonical Allele Identifier: CA1950237317
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616772G= , CM000673.2:g.6616772G= GRCh38
NC_000011.9:g.6638003G= , CM000673.1:g.6638003G= GRCh37
NC_000011.8:g.6594579G= NCBI36
NG_008653.1:g.7690C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.661C= ENSP00000507321.1:p.Arg221=
ENST00000299427.12:c.775C= MANE Select ENSP00000299427.6:p.Arg259=
ENST00000436873.7:c.312+529C=
ENST00000524788.2:n.1934C=
ENST00000524903.2:n.2050C=
ENST00000528807.2:n.431C=
ENST00000530040.2:n.480-269C=
ENST00000533371.6:c.46C= ENSP00000437066.1:p.Arg16=
ENST00000642892.1:c.46C= ENSP00000494165.1:p.Arg16=
ENST00000643439.1:c.*515C= ENSP00000495849.1:n.*515C=
ENST00000643479.1:n.804C=
ENST00000643516.1:c.396-269C=
ENST00000644151.1:n.2214C=
ENST00000644218.1:c.775C= ENSP00000493574.1:p.Arg259=
ENST00000644683.1:c.*228C= ENSP00000494085.1:n.*228C=
ENST00000644810.1:c.496C= ENSP00000495895.1:p.Arg166=
ENST00000644831.1:n.951C=
ENST00000644933.1:c.46C= ENSP00000496133.1:p.Arg16=
ENST00000645020.1:n.2065C=
ENST00000645285.1:c.46C= ENSP00000495058.1:p.Arg16=
ENST00000645331.1:n.1141C=
ENST00000645620.1:c.46C= ENSP00000493657.1:p.Arg16=
ENST00000646777.1:n.951C=
ENST00000647016.1:n.1255C=
ENST00000647152.1:c.46C= ENSP00000495893.1:p.Arg16=
ENST00000647209.1:c.*644C= ENSP00000495558.1:n.*644C=
ENST00000647346.1:n.1795C=
ENST00000299427.10:c.775C= ENSP00000299427.6:p.Arg259=
ENST00000436873.6:c.451-269C= ENSP00000398136.2:n.451-269C=
ENST00000524788.1:n.475C=
ENST00000528807.1:n.325C=
ENST00000533371.5:c.46C= ENSP00000437066.1:p.Arg16=
ENST00000611494.4:c.775C= ENSP00000484546.1:p.Arg259=
NM_000391.3:c.775C= NP_000382.3:p.Arg259=
NM_000391.4:c.775C= MANE Select NP_000382.3:p.Arg259=