Canonical Allele Identifier: CA1950215351
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617728G= , CM000673.2:g.6617728G= GRCh38
NC_000011.9:g.6638959G= , CM000673.1:g.6638959G= GRCh37
NC_000011.8:g.6595535G= NCBI36
NG_008653.1:g.6734C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.164C= ENSP00000507321.1:p.Pro55=
ENST00000299427.12:c.278C= MANE Select ENSP00000299427.6:p.Pro93=
ENST00000428886.7:n.366C=
ENST00000436873.7:c.82C=
ENST00000524788.2:n.1290C=
ENST00000524903.2:n.1406C=
ENST00000528571.6:c.*18C= ENSP00000434647.1:n.*18C=
ENST00000530040.2:n.307C=
ENST00000533371.6:c.-452C= ENSP00000437066.1:n.-452C=
ENST00000534644.6:n.279C=
ENST00000642892.1:c.-399C= ENSP00000494165.1:n.-399C=
ENST00000643439.1:c.*18C= ENSP00000495849.1:n.*18C=
ENST00000643479.1:n.307C=
ENST00000643516.1:c.165C=
ENST00000644151.1:n.1570C=
ENST00000644218.1:c.278C= ENSP00000493574.1:p.Pro93=
ENST00000644683.1:c.278C= ENSP00000494085.1:p.Pro93=
ENST00000644810.1:c.230-575C= ENSP00000495895.1:n.230-575C=
ENST00000644831.1:n.307C=
ENST00000644933.1:c.-452C= ENSP00000496133.1:n.-452C=
ENST00000645020.1:n.1306C=
ENST00000645285.1:c.-452C= ENSP00000495058.1:n.-452C=
ENST00000645331.1:n.300C=
ENST00000645620.1:c.-394C= ENSP00000493657.1:n.-394C=
ENST00000646777.1:n.307C=
ENST00000647016.1:n.611C=
ENST00000647152.1:c.-452C= ENSP00000495893.1:n.-452C=
ENST00000647209.1:c.*147C= ENSP00000495558.1:n.*147C=
ENST00000647346.1:n.1298C=
ENST00000299427.10:c.278C= ENSP00000299427.6:p.Pro93=
ENST00000428886.6:n.300C=
ENST00000436873.6:c.278C= ENSP00000398136.2:p.Pro93=
ENST00000528571.5:c.*18C= ENSP00000434647.1:n.*18C=
ENST00000530040.1:n.390C=
ENST00000533371.5:c.-452C= ENSP00000437066.1:n.-452C=
ENST00000534644.5:n.263C=
ENST00000611494.4:c.278C= ENSP00000484546.1:p.Pro93=
NM_000391.3:c.278C= NP_000382.3:p.Pro93=
NM_000391.4:c.278C= MANE Select NP_000382.3:p.Pro93=