Canonical Allele Identifier: CA379476184
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617644G>T , CM000673.2:g.6617644G>T GRCh38
NC_000011.9:g.6638875G>T , CM000673.1:g.6638875G>T GRCh37
NC_000011.8:g.6595451G>T NCBI36
NG_008653.1:g.6818C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.248C>A ENSP00000507321.1:p.Thr83Asn
ENST00000299427.12:c.362C>A MANE Select ENSP00000299427.6:p.Thr121Asn
ENST00000428886.7:n.450C>A
ENST00000436873.7:c.166C>A
ENST00000524788.2:n.1374C>A
ENST00000524903.2:n.1490C>A
ENST00000528571.6:c.*102C>A ENSP00000434647.1:n.*102C>A
ENST00000530040.2:n.391C>A
ENST00000533371.6:c.-368C>A ENSP00000437066.1:n.-368C>A
ENST00000534644.6:n.363C>A
ENST00000642892.1:c.-315C>A ENSP00000494165.1:n.-315C>A
ENST00000643439.1:c.*102C>A ENSP00000495849.1:n.*102C>A
ENST00000643479.1:n.391C>A
ENST00000643516.1:c.249C>A
ENST00000644151.1:n.1654C>A
ENST00000644218.1:c.362C>A ENSP00000493574.1:p.Thr121Asn
ENST00000644683.1:c.362C>A ENSP00000494085.1:p.Thr121Asn
ENST00000644810.1:c.230-491C>A ENSP00000495895.1:n.230-491C>A
ENST00000644831.1:n.391C>A
ENST00000644933.1:c.-368C>A ENSP00000496133.1:n.-368C>A
ENST00000645020.1:n.1390C>A
ENST00000645285.1:c.-368C>A ENSP00000495058.1:n.-368C>A
ENST00000645331.1:n.384C>A
ENST00000645620.1:c.-310C>A ENSP00000493657.1:n.-310C>A
ENST00000646777.1:n.391C>A
ENST00000647016.1:n.695C>A
ENST00000647152.1:c.-368C>A ENSP00000495893.1:n.-368C>A
ENST00000647209.1:c.*231C>A ENSP00000495558.1:n.*231C>A
ENST00000647346.1:n.1382C>A
ENST00000299427.10:c.362C>A ENSP00000299427.6:p.Thr121Asn
ENST00000428886.6:n.384C>A
ENST00000436873.6:c.362C>A ENSP00000398136.2:p.Thr121Asn
ENST00000528571.5:c.*102C>A ENSP00000434647.1:n.*102C>A
ENST00000530040.1:n.474C>A
ENST00000533371.5:c.-368C>A ENSP00000437066.1:n.-368C>A
ENST00000534644.5:n.347C>A
ENST00000611494.4:c.362C>A ENSP00000484546.1:p.Thr121Asn
NM_000391.3:c.362C>A NP_000382.3:p.Thr121Asn
NM_000391.4:c.362C>A MANE Select NP_000382.3:p.Thr121Asn