Canonical Allele Identifier: CA379475630
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617138C>G , CM000673.2:g.6617138C>G GRCh38
NC_000011.9:g.6638369C>G , CM000673.1:g.6638369C>G GRCh37
NC_000011.8:g.6594945C>G NCBI36
NG_008653.1:g.7324G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.410G>C ENSP00000507321.1:p.Arg137Pro
ENST00000299427.12:c.524G>C MANE Select ENSP00000299427.6:p.Arg175Pro
ENST00000428886.7:n.759G>C
ENST00000436873.7:c.312+163G>C
ENST00000524788.2:n.1683G>C
ENST00000524903.2:n.1799G>C
ENST00000528807.2:n.180G>C
ENST00000530040.2:n.479+221G>C
ENST00000533371.6:c.-206G>C ENSP00000437066.1:n.-206G>C
ENST00000534644.6:n.472G>C
ENST00000642892.1:c.-206G>C ENSP00000494165.1:n.-206G>C
ENST00000643439.1:c.*264G>C ENSP00000495849.1:n.*264G>C
ENST00000643479.1:n.553G>C
ENST00000643516.1:c.395+163G>C
ENST00000644151.1:n.1963G>C
ENST00000644218.1:c.524G>C ENSP00000493574.1:p.Arg175Pro
ENST00000644683.1:c.466G>C ENSP00000494085.1:p.Val156Leu
ENST00000644810.1:c.245G>C ENSP00000495895.1:p.Arg82Pro
ENST00000644831.1:n.700G>C
ENST00000644933.1:c.-206G>C ENSP00000496133.1:n.-206G>C
ENST00000645020.1:n.1699G>C
ENST00000645285.1:c.-206G>C ENSP00000495058.1:n.-206G>C
ENST00000645331.1:n.890G>C
ENST00000645620.1:c.-206G>C ENSP00000493657.1:n.-206G>C
ENST00000646777.1:n.700G>C
ENST00000647016.1:n.1004G>C
ENST00000647152.1:c.-206G>C ENSP00000495893.1:n.-206G>C
ENST00000647209.1:c.*393G>C ENSP00000495558.1:n.*393G>C
ENST00000647346.1:n.1544G>C
ENST00000299427.10:c.524G>C ENSP00000299427.6:p.Arg175Pro
ENST00000428886.6:n.693G>C
ENST00000436873.6:c.450+221G>C ENSP00000398136.2:n.450+221G>C
ENST00000524788.1:n.224G>C
ENST00000528571.5:c.*264G>C ENSP00000434647.1:n.*264G>C
ENST00000528807.1:n.74G>C
ENST00000533371.5:c.-206G>C ENSP00000437066.1:n.-206G>C
ENST00000534644.5:n.509G>C
ENST00000611494.4:c.524G>C ENSP00000484546.1:p.Arg175Pro
NM_000391.3:c.524G>C NP_000382.3:p.Arg175Pro
NM_000391.4:c.524G>C MANE Select NP_000382.3:p.Arg175Pro