Canonical Allele Identifier: CA379476329
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617681G>C , CM000673.2:g.6617681G>C GRCh38
NC_000011.9:g.6638912G>C , CM000673.1:g.6638912G>C GRCh37
NC_000011.8:g.6595488G>C NCBI36
NG_008653.1:g.6781C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.211C>G ENSP00000507321.1:p.Gln71Glu
ENST00000299427.12:c.325C>G MANE Select ENSP00000299427.6:p.Gln109Glu
ENST00000428886.7:n.413C>G
ENST00000436873.7:c.129C>G
ENST00000524788.2:n.1337C>G
ENST00000524903.2:n.1453C>G
ENST00000528571.6:c.*65C>G ENSP00000434647.1:n.*65C>G
ENST00000530040.2:n.354C>G
ENST00000533371.6:c.-405C>G ENSP00000437066.1:n.-405C>G
ENST00000534644.6:n.326C>G
ENST00000642892.1:c.-352C>G ENSP00000494165.1:n.-352C>G
ENST00000643439.1:c.*65C>G ENSP00000495849.1:n.*65C>G
ENST00000643479.1:n.354C>G
ENST00000643516.1:c.212C>G
ENST00000644151.1:n.1617C>G
ENST00000644218.1:c.325C>G ENSP00000493574.1:p.Gln109Glu
ENST00000644683.1:c.325C>G ENSP00000494085.1:p.Gln109Glu
ENST00000644810.1:c.230-528C>G ENSP00000495895.1:n.230-528C>G
ENST00000644831.1:n.354C>G
ENST00000644933.1:c.-405C>G ENSP00000496133.1:n.-405C>G
ENST00000645020.1:n.1353C>G
ENST00000645285.1:c.-405C>G ENSP00000495058.1:n.-405C>G
ENST00000645331.1:n.347C>G
ENST00000645620.1:c.-347C>G ENSP00000493657.1:n.-347C>G
ENST00000646777.1:n.354C>G
ENST00000647016.1:n.658C>G
ENST00000647152.1:c.-405C>G ENSP00000495893.1:n.-405C>G
ENST00000647209.1:c.*194C>G ENSP00000495558.1:n.*194C>G
ENST00000647346.1:n.1345C>G
ENST00000299427.10:c.325C>G ENSP00000299427.6:p.Gln109Glu
ENST00000428886.6:n.347C>G
ENST00000436873.6:c.325C>G ENSP00000398136.2:p.Gln109Glu
ENST00000528571.5:c.*65C>G ENSP00000434647.1:n.*65C>G
ENST00000530040.1:n.437C>G
ENST00000533371.5:c.-405C>G ENSP00000437066.1:n.-405C>G
ENST00000534644.5:n.310C>G
ENST00000611494.4:c.325C>G ENSP00000484546.1:p.Gln109Glu
NM_000391.3:c.325C>G NP_000382.3:p.Gln109Glu
NM_000391.4:c.325C>G MANE Select NP_000382.3:p.Gln109Glu