Canonical Allele Identifier: CA1950215316
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617708G= , CM000673.2:g.6617708G= GRCh38
NC_000011.9:g.6638939G= , CM000673.1:g.6638939G= GRCh37
NC_000011.8:g.6595515G= NCBI36
NG_008653.1:g.6754C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.184C= ENSP00000507321.1:p.Gln62=
ENST00000299427.12:c.298C= MANE Select ENSP00000299427.6:p.Gln100=
ENST00000428886.7:n.386C=
ENST00000436873.7:c.102C=
ENST00000524788.2:n.1310C=
ENST00000524903.2:n.1426C=
ENST00000528571.6:c.*38C= ENSP00000434647.1:n.*38C=
ENST00000530040.2:n.327C=
ENST00000533371.6:c.-432C= ENSP00000437066.1:n.-432C=
ENST00000534644.6:n.299C=
ENST00000642892.1:c.-379C= ENSP00000494165.1:n.-379C=
ENST00000643439.1:c.*38C= ENSP00000495849.1:n.*38C=
ENST00000643479.1:n.327C=
ENST00000643516.1:c.185C=
ENST00000644151.1:n.1590C=
ENST00000644218.1:c.298C= ENSP00000493574.1:p.Gln100=
ENST00000644683.1:c.298C= ENSP00000494085.1:p.Gln100=
ENST00000644810.1:c.230-555C= ENSP00000495895.1:n.230-555C=
ENST00000644831.1:n.327C=
ENST00000644933.1:c.-432C= ENSP00000496133.1:n.-432C=
ENST00000645020.1:n.1326C=
ENST00000645285.1:c.-432C= ENSP00000495058.1:n.-432C=
ENST00000645331.1:n.320C=
ENST00000645620.1:c.-374C= ENSP00000493657.1:n.-374C=
ENST00000646777.1:n.327C=
ENST00000647016.1:n.631C=
ENST00000647152.1:c.-432C= ENSP00000495893.1:n.-432C=
ENST00000647209.1:c.*167C= ENSP00000495558.1:n.*167C=
ENST00000647346.1:n.1318C=
ENST00000299427.10:c.298C= ENSP00000299427.6:p.Gln100=
ENST00000428886.6:n.320C=
ENST00000436873.6:c.298C= ENSP00000398136.2:p.Gln100=
ENST00000528571.5:c.*38C= ENSP00000434647.1:n.*38C=
ENST00000530040.1:n.410C=
ENST00000533371.5:c.-432C= ENSP00000437066.1:n.-432C=
ENST00000534644.5:n.283C=
ENST00000611494.4:c.298C= ENSP00000484546.1:p.Gln100=
NM_000391.3:c.298C= NP_000382.3:p.Gln100=
NM_000391.4:c.298C= MANE Select NP_000382.3:p.Gln100=