Canonical Allele Identifier: CA1950214878
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617347T= , CM000673.2:g.6617347T= GRCh38
NC_000011.9:g.6638578T= , CM000673.1:g.6638578T= GRCh37
NC_000011.8:g.6595154T= NCBI36
NG_008653.1:g.7115A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.348A= ENSP00000507321.1:p.Pro116=
ENST00000299427.12:c.462A= MANE Select ENSP00000299427.6:p.Pro154=
ENST00000428886.7:n.550A=
ENST00000436873.7:c.266A=
ENST00000524788.2:n.1474A=
ENST00000524903.2:n.1590A=
ENST00000528571.6:c.*202A= ENSP00000434647.1:n.*202A=
ENST00000528807.2:n.118A=
ENST00000530040.2:n.479+12A=
ENST00000533371.6:c.-268A= ENSP00000437066.1:n.-268A=
ENST00000534644.6:n.456+7A=
ENST00000642892.1:c.-222+7A= ENSP00000494165.1:n.-222+7A=
ENST00000643439.1:c.*202A= ENSP00000495849.1:n.*202A=
ENST00000643479.1:n.491A=
ENST00000643516.1:c.349A=
ENST00000644151.1:n.1754A=
ENST00000644218.1:c.462A= ENSP00000493574.1:p.Pro154=
ENST00000644683.1:c.450+12A= ENSP00000494085.1:n.450+12A=
ENST00000644810.1:c.230-194A= ENSP00000495895.1:n.230-194A=
ENST00000644831.1:n.491A=
ENST00000644933.1:c.-268A= ENSP00000496133.1:n.-268A=
ENST00000645020.1:n.1490A=
ENST00000645285.1:c.-268A= ENSP00000495058.1:n.-268A=
ENST00000645331.1:n.681A=
ENST00000645620.1:c.-222+12A= ENSP00000493657.1:n.-222+12A=
ENST00000646777.1:n.491A=
ENST00000647016.1:n.795A=
ENST00000647152.1:c.-268A= ENSP00000495893.1:n.-268A=
ENST00000647209.1:c.*331A= ENSP00000495558.1:n.*331A=
ENST00000647346.1:n.1482A=
ENST00000299427.10:c.462A= ENSP00000299427.6:p.Pro154=
ENST00000428886.6:n.484A=
ENST00000436873.6:c.450+12A= ENSP00000398136.2:n.450+12A=
ENST00000524788.1:n.15A=
ENST00000528571.5:c.*202A= ENSP00000434647.1:n.*202A=
ENST00000533371.5:c.-268A= ENSP00000437066.1:n.-268A=
ENST00000534644.5:n.447A=
ENST00000611494.4:c.462A= ENSP00000484546.1:p.Pro154=
NM_000391.3:c.462A= NP_000382.3:p.Pro154=
NM_000391.4:c.462A= MANE Select NP_000382.3:p.Pro154=