Canonical Allele Identifier: CA379476356
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617689G>C , CM000673.2:g.6617689G>C GRCh38
NC_000011.9:g.6638920G>C , CM000673.1:g.6638920G>C GRCh37
NC_000011.8:g.6595496G>C NCBI36
NG_008653.1:g.6773C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.203C>G ENSP00000507321.1:p.Ala68Gly
ENST00000299427.12:c.317C>G MANE Select ENSP00000299427.6:p.Ala106Gly
ENST00000428886.7:n.405C>G
ENST00000436873.7:c.121C>G
ENST00000524788.2:n.1329C>G
ENST00000524903.2:n.1445C>G
ENST00000528571.6:c.*57C>G ENSP00000434647.1:n.*57C>G
ENST00000530040.2:n.346C>G
ENST00000533371.6:c.-413C>G ENSP00000437066.1:n.-413C>G
ENST00000534644.6:n.318C>G
ENST00000642892.1:c.-360C>G ENSP00000494165.1:n.-360C>G
ENST00000643439.1:c.*57C>G ENSP00000495849.1:n.*57C>G
ENST00000643479.1:n.346C>G
ENST00000643516.1:c.204C>G
ENST00000644151.1:n.1609C>G
ENST00000644218.1:c.317C>G ENSP00000493574.1:p.Ala106Gly
ENST00000644683.1:c.317C>G ENSP00000494085.1:p.Ala106Gly
ENST00000644810.1:c.230-536C>G ENSP00000495895.1:n.230-536C>G
ENST00000644831.1:n.346C>G
ENST00000644933.1:c.-413C>G ENSP00000496133.1:n.-413C>G
ENST00000645020.1:n.1345C>G
ENST00000645285.1:c.-413C>G ENSP00000495058.1:n.-413C>G
ENST00000645331.1:n.339C>G
ENST00000645620.1:c.-355C>G ENSP00000493657.1:n.-355C>G
ENST00000646777.1:n.346C>G
ENST00000647016.1:n.650C>G
ENST00000647152.1:c.-413C>G ENSP00000495893.1:n.-413C>G
ENST00000647209.1:c.*186C>G ENSP00000495558.1:n.*186C>G
ENST00000647346.1:n.1337C>G
ENST00000299427.10:c.317C>G ENSP00000299427.6:p.Ala106Gly
ENST00000428886.6:n.339C>G
ENST00000436873.6:c.317C>G ENSP00000398136.2:p.Ala106Gly
ENST00000528571.5:c.*57C>G ENSP00000434647.1:n.*57C>G
ENST00000530040.1:n.429C>G
ENST00000533371.5:c.-413C>G ENSP00000437066.1:n.-413C>G
ENST00000534644.5:n.302C>G
ENST00000611494.4:c.317C>G ENSP00000484546.1:p.Ala106Gly
NM_000391.3:c.317C>G NP_000382.3:p.Ala106Gly
NM_000391.4:c.317C>G MANE Select NP_000382.3:p.Ala106Gly