Canonical Allele Identifier: CA379476488
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617720G>C , CM000673.2:g.6617720G>C GRCh38
NC_000011.9:g.6638951G>C , CM000673.1:g.6638951G>C GRCh37
NC_000011.8:g.6595527G>C NCBI36
NG_008653.1:g.6742C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.172C>G ENSP00000507321.1:p.Leu58Val
ENST00000299427.12:c.286C>G MANE Select ENSP00000299427.6:p.Leu96Val
ENST00000428886.7:n.374C>G
ENST00000436873.7:c.90C>G
ENST00000524788.2:n.1298C>G
ENST00000524903.2:n.1414C>G
ENST00000528571.6:c.*26C>G ENSP00000434647.1:n.*26C>G
ENST00000530040.2:n.315C>G
ENST00000533371.6:c.-444C>G ENSP00000437066.1:n.-444C>G
ENST00000534644.6:n.287C>G
ENST00000642892.1:c.-391C>G ENSP00000494165.1:n.-391C>G
ENST00000643439.1:c.*26C>G ENSP00000495849.1:n.*26C>G
ENST00000643479.1:n.315C>G
ENST00000643516.1:c.173C>G
ENST00000644151.1:n.1578C>G
ENST00000644218.1:c.286C>G ENSP00000493574.1:p.Leu96Val
ENST00000644683.1:c.286C>G ENSP00000494085.1:p.Leu96Val
ENST00000644810.1:c.230-567C>G ENSP00000495895.1:n.230-567C>G
ENST00000644831.1:n.315C>G
ENST00000644933.1:c.-444C>G ENSP00000496133.1:n.-444C>G
ENST00000645020.1:n.1314C>G
ENST00000645285.1:c.-444C>G ENSP00000495058.1:n.-444C>G
ENST00000645331.1:n.308C>G
ENST00000645620.1:c.-386C>G ENSP00000493657.1:n.-386C>G
ENST00000646777.1:n.315C>G
ENST00000647016.1:n.619C>G
ENST00000647152.1:c.-444C>G ENSP00000495893.1:n.-444C>G
ENST00000647209.1:c.*155C>G ENSP00000495558.1:n.*155C>G
ENST00000647346.1:n.1306C>G
ENST00000299427.10:c.286C>G ENSP00000299427.6:p.Leu96Val
ENST00000428886.6:n.308C>G
ENST00000436873.6:c.286C>G ENSP00000398136.2:p.Leu96Val
ENST00000528571.5:c.*26C>G ENSP00000434647.1:n.*26C>G
ENST00000530040.1:n.398C>G
ENST00000533371.5:c.-444C>G ENSP00000437066.1:n.-444C>G
ENST00000534644.5:n.271C>G
ENST00000611494.4:c.286C>G ENSP00000484546.1:p.Leu96Val
NM_000391.3:c.286C>G NP_000382.3:p.Leu96Val
NM_000391.4:c.286C>G MANE Select NP_000382.3:p.Leu96Val