Canonical Allele Identifier: CA1950237836
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617037A= , CM000673.2:g.6617037A= GRCh38
NC_000011.9:g.6638268A= , CM000673.1:g.6638268A= GRCh37
NC_000011.8:g.6594844A= NCBI36
NG_008653.1:g.7425T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.511T= ENSP00000507321.1:p.Tyr171=
ENST00000299427.12:c.625T= MANE Select ENSP00000299427.6:p.Tyr209=
ENST00000436873.7:c.312+264T=
ENST00000524788.2:n.1784T=
ENST00000524903.2:n.1900T=
ENST00000528807.2:n.281T=
ENST00000530040.2:n.479+322T=
ENST00000533371.6:c.-105T= ENSP00000437066.1:n.-105T=
ENST00000534644.6:n.573T=
ENST00000642892.1:c.-105T= ENSP00000494165.1:n.-105T=
ENST00000643439.1:c.*365T= ENSP00000495849.1:n.*365T=
ENST00000643479.1:n.654T=
ENST00000643516.1:c.395+264T=
ENST00000644151.1:n.2064T=
ENST00000644218.1:c.625T= ENSP00000493574.1:p.Tyr209=
ENST00000644683.1:c.*78T= ENSP00000494085.1:n.*78T=
ENST00000644810.1:c.346T= ENSP00000495895.1:p.Tyr116=
ENST00000644831.1:n.801T=
ENST00000644933.1:c.-105T= ENSP00000496133.1:n.-105T=
ENST00000645020.1:n.1800T=
ENST00000645285.1:c.-105T= ENSP00000495058.1:n.-105T=
ENST00000645331.1:n.991T=
ENST00000645620.1:c.-105T= ENSP00000493657.1:n.-105T=
ENST00000646777.1:n.801T=
ENST00000647016.1:n.1105T=
ENST00000647152.1:c.-105T= ENSP00000495893.1:n.-105T=
ENST00000647209.1:c.*494T= ENSP00000495558.1:n.*494T=
ENST00000647346.1:n.1645T=
ENST00000299427.10:c.625T= ENSP00000299427.6:p.Tyr209=
ENST00000428886.6:n.794T=
ENST00000436873.6:c.450+322T= ENSP00000398136.2:n.450+322T=
ENST00000524788.1:n.325T=
ENST00000528571.5:c.*365T= ENSP00000434647.1:n.*365T=
ENST00000528807.1:n.175T=
ENST00000533371.5:c.-105T= ENSP00000437066.1:n.-105T=
ENST00000534644.5:n.610T=
ENST00000611494.4:c.625T= ENSP00000484546.1:p.Tyr209=
NM_000391.3:c.625T= NP_000382.3:p.Tyr209=
NM_000391.4:c.625T= MANE Select NP_000382.3:p.Tyr209=