Canonical Allele Identifier: CA1950237388
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616813C= , CM000673.2:g.6616813C= GRCh38
NC_000011.9:g.6638044C= , CM000673.1:g.6638044C= GRCh37
NC_000011.8:g.6594620C= NCBI36
NG_008653.1:g.7649G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.620G= ENSP00000507321.1:p.Arg207=
ENST00000299427.12:c.734G= MANE Select ENSP00000299427.6:p.Arg245=
ENST00000436873.7:c.312+488G=
ENST00000524788.2:n.1893G=
ENST00000524903.2:n.2009G=
ENST00000528807.2:n.390G=
ENST00000530040.2:n.480-310G=
ENST00000533371.6:c.5G= ENSP00000437066.1:p.Arg2=
ENST00000642892.1:c.5G= ENSP00000494165.1:p.Arg2=
ENST00000643439.1:c.*474G= ENSP00000495849.1:n.*474G=
ENST00000643479.1:n.763G=
ENST00000643516.1:c.396-310G=
ENST00000644151.1:n.2173G=
ENST00000644218.1:c.734G= ENSP00000493574.1:p.Arg245=
ENST00000644683.1:c.*187G= ENSP00000494085.1:n.*187G=
ENST00000644810.1:c.455G= ENSP00000495895.1:p.Arg152=
ENST00000644831.1:n.910G=
ENST00000644933.1:c.5G= ENSP00000496133.1:p.Arg2=
ENST00000645020.1:n.2024G=
ENST00000645285.1:c.5G= ENSP00000495058.1:p.Arg2=
ENST00000645331.1:n.1100G=
ENST00000645620.1:c.5G= ENSP00000493657.1:p.Arg2=
ENST00000646777.1:n.910G=
ENST00000647016.1:n.1214G=
ENST00000647152.1:c.5G= ENSP00000495893.1:p.Arg2=
ENST00000647209.1:c.*603G= ENSP00000495558.1:n.*603G=
ENST00000647346.1:n.1754G=
ENST00000299427.10:c.734G= ENSP00000299427.6:p.Arg245=
ENST00000436873.6:c.451-310G= ENSP00000398136.2:n.451-310G=
ENST00000524788.1:n.434G=
ENST00000528807.1:n.284G=
ENST00000533371.5:c.5G= ENSP00000437066.1:p.Arg2=
ENST00000611494.4:c.734G= ENSP00000484546.1:p.Arg245=
NM_000391.3:c.734G= NP_000382.3:p.Arg245=
NM_000391.4:c.734G= MANE Select NP_000382.3:p.Arg245=