Canonical Allele Identifier: CA1950237688
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616983A= , CM000673.2:g.6616983A= GRCh38
NC_000011.9:g.6638214A= , CM000673.1:g.6638214A= GRCh37
NC_000011.8:g.6594790A= NCBI36
NG_008653.1:g.7479T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.565T= ENSP00000507321.1:p.Cys189=
ENST00000299427.12:c.679T= MANE Select ENSP00000299427.6:p.Cys227=
ENST00000436873.7:c.312+318T=
ENST00000524788.2:n.1838T=
ENST00000524903.2:n.1954T=
ENST00000528807.2:n.335T=
ENST00000530040.2:n.479+376T=
ENST00000533371.6:c.-51T= ENSP00000437066.1:n.-51T=
ENST00000534644.6:n.627T=
ENST00000642892.1:c.-51T= ENSP00000494165.1:n.-51T=
ENST00000643439.1:c.*419T= ENSP00000495849.1:n.*419T=
ENST00000643479.1:n.708T=
ENST00000643516.1:c.395+318T=
ENST00000644151.1:n.2118T=
ENST00000644218.1:c.679T= ENSP00000493574.1:p.Cys227=
ENST00000644683.1:c.*132T= ENSP00000494085.1:n.*132T=
ENST00000644810.1:c.400T= ENSP00000495895.1:p.Cys134=
ENST00000644831.1:n.855T=
ENST00000644933.1:c.-51T= ENSP00000496133.1:n.-51T=
ENST00000645020.1:n.1854T=
ENST00000645285.1:c.-51T= ENSP00000495058.1:n.-51T=
ENST00000645331.1:n.1045T=
ENST00000645620.1:c.-51T= ENSP00000493657.1:n.-51T=
ENST00000646777.1:n.855T=
ENST00000647016.1:n.1159T=
ENST00000647152.1:c.-51T= ENSP00000495893.1:n.-51T=
ENST00000647209.1:c.*548T= ENSP00000495558.1:n.*548T=
ENST00000647346.1:n.1699T=
ENST00000299427.10:c.679T= ENSP00000299427.6:p.Cys227=
ENST00000436873.6:c.450+376T= ENSP00000398136.2:n.450+376T=
ENST00000524788.1:n.379T=
ENST00000528571.5:c.*419T= ENSP00000434647.1:n.*419T=
ENST00000528807.1:n.229T=
ENST00000533371.5:c.-51T= ENSP00000437066.1:n.-51T=
ENST00000611494.4:c.679T= ENSP00000484546.1:p.Cys227=
NM_000391.3:c.679T= NP_000382.3:p.Cys227=
NM_000391.4:c.679T= MANE Select NP_000382.3:p.Cys227=