Canonical Allele Identifier: CA1950214884
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617352A= , CM000673.2:g.6617352A= GRCh38
NC_000011.9:g.6638583A= , CM000673.1:g.6638583A= GRCh37
NC_000011.8:g.6595159A= NCBI36
NG_008653.1:g.7110T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.343T= ENSP00000507321.1:p.Ser115=
ENST00000299427.12:c.457T= MANE Select ENSP00000299427.6:p.Ser153=
ENST00000428886.7:n.545T=
ENST00000436873.7:c.261T=
ENST00000524788.2:n.1469T=
ENST00000524903.2:n.1585T=
ENST00000528571.6:c.*197T= ENSP00000434647.1:n.*197T=
ENST00000528807.2:n.113T=
ENST00000530040.2:n.479+7T=
ENST00000533371.6:c.-273T= ENSP00000437066.1:n.-273T=
ENST00000534644.6:n.456+2T=
ENST00000642892.1:c.-222+2T= ENSP00000494165.1:n.-222+2T=
ENST00000643439.1:c.*197T= ENSP00000495849.1:n.*197T=
ENST00000643479.1:n.486T=
ENST00000643516.1:c.344T=
ENST00000644151.1:n.1749T=
ENST00000644218.1:c.457T= ENSP00000493574.1:p.Ser153=
ENST00000644683.1:c.450+7T= ENSP00000494085.1:n.450+7T=
ENST00000644810.1:c.230-199T= ENSP00000495895.1:n.230-199T=
ENST00000644831.1:n.486T=
ENST00000644933.1:c.-273T= ENSP00000496133.1:n.-273T=
ENST00000645020.1:n.1485T=
ENST00000645285.1:c.-273T= ENSP00000495058.1:n.-273T=
ENST00000645331.1:n.676T=
ENST00000645620.1:c.-222+7T= ENSP00000493657.1:n.-222+7T=
ENST00000646777.1:n.486T=
ENST00000647016.1:n.790T=
ENST00000647152.1:c.-273T= ENSP00000495893.1:n.-273T=
ENST00000647209.1:c.*326T= ENSP00000495558.1:n.*326T=
ENST00000647346.1:n.1477T=
ENST00000299427.10:c.457T= ENSP00000299427.6:p.Ser153=
ENST00000428886.6:n.479T=
ENST00000436873.6:c.450+7T= ENSP00000398136.2:n.450+7T=
ENST00000524788.1:n.10T=
ENST00000528571.5:c.*197T= ENSP00000434647.1:n.*197T=
ENST00000533371.5:c.-273T= ENSP00000437066.1:n.-273T=
ENST00000534644.5:n.442T=
ENST00000611494.4:c.457T= ENSP00000484546.1:p.Ser153=
NM_000391.3:c.457T= NP_000382.3:p.Ser153=
NM_000391.4:c.457T= MANE Select NP_000382.3:p.Ser153=