Canonical Allele Identifier: CA1950238397
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617274A= , CM000673.2:g.6617274A= GRCh38
NC_000011.9:g.6638505A= , CM000673.1:g.6638505A= GRCh37
NC_000011.8:g.6595081A= NCBI36
NG_008653.1:g.7188T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.394+27T= ENSP00000507321.1:n.394+27T=
ENST00000299427.12:c.508+27T= MANE Select ENSP00000299427.6:n.508+27T=
ENST00000428886.7:n.623T=
ENST00000436873.7:c.312+27T=
ENST00000524788.2:n.1547T=
ENST00000524903.2:n.1663T=
ENST00000528571.6:c.*275T= ENSP00000434647.1:n.*275T=
ENST00000528807.2:n.164+27T=
ENST00000530040.2:n.479+85T=
ENST00000533371.6:c.-222+27T= ENSP00000437066.1:n.-222+27T=
ENST00000534644.6:n.456+80T=
ENST00000642892.1:c.-222+80T= ENSP00000494165.1:n.-222+80T=
ENST00000643439.1:c.*248+27T= ENSP00000495849.1:n.*248+27T=
ENST00000643479.1:n.537+27T=
ENST00000643516.1:c.395+27T=
ENST00000644151.1:n.1827T=
ENST00000644218.1:c.508+27T= ENSP00000493574.1:n.508+27T=
ENST00000644683.1:c.450+85T= ENSP00000494085.1:n.450+85T=
ENST00000644810.1:c.230-121T= ENSP00000495895.1:n.230-121T=
ENST00000644831.1:n.564T=
ENST00000644933.1:c.-222+27T= ENSP00000496133.1:n.-222+27T=
ENST00000645020.1:n.1563T=
ENST00000645285.1:c.-222+27T= ENSP00000495058.1:n.-222+27T=
ENST00000645331.1:n.754T=
ENST00000645620.1:c.-222+85T= ENSP00000493657.1:n.-222+85T=
ENST00000646777.1:n.564T=
ENST00000647016.1:n.868T=
ENST00000647152.1:c.-222+27T= ENSP00000495893.1:n.-222+27T=
ENST00000647209.1:c.*377+27T= ENSP00000495558.1:n.*377+27T=
ENST00000647346.1:n.1528+27T=
ENST00000299427.10:c.508+27T= ENSP00000299427.6:n.508+27T=
ENST00000428886.6:n.557T=
ENST00000436873.6:c.450+85T= ENSP00000398136.2:n.450+85T=
ENST00000524788.1:n.88T=
ENST00000528571.5:c.*248+27T= ENSP00000434647.1:n.*248+27T=
ENST00000533371.5:c.-222+27T= ENSP00000437066.1:n.-222+27T=
ENST00000534644.5:n.493+27T=
ENST00000611494.4:c.508+27T= ENSP00000484546.1:n.508+27T=
NM_000391.3:c.508+27T= NP_000382.3:n.508+27T=
NM_000391.4:c.508+27T= MANE Select NP_000382.3:n.508+27T=