Canonical Allele Identifier: CA379476515
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617729G>T , CM000673.2:g.6617729G>T GRCh38
NC_000011.9:g.6638960G>T , CM000673.1:g.6638960G>T GRCh37
NC_000011.8:g.6595536G>T NCBI36
NG_008653.1:g.6733C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.163C>A ENSP00000507321.1:p.Pro55Thr
ENST00000299427.12:c.277C>A MANE Select ENSP00000299427.6:p.Pro93Thr
ENST00000428886.7:n.365C>A
ENST00000436873.7:c.81C>A
ENST00000524788.2:n.1289C>A
ENST00000524903.2:n.1405C>A
ENST00000528571.6:c.*17C>A ENSP00000434647.1:n.*17C>A
ENST00000530040.2:n.306C>A
ENST00000533371.6:c.-453C>A ENSP00000437066.1:n.-453C>A
ENST00000534644.6:n.278C>A
ENST00000642892.1:c.-400C>A ENSP00000494165.1:n.-400C>A
ENST00000643439.1:c.*17C>A ENSP00000495849.1:n.*17C>A
ENST00000643479.1:n.306C>A
ENST00000643516.1:c.164C>A
ENST00000644151.1:n.1569C>A
ENST00000644218.1:c.277C>A ENSP00000493574.1:p.Pro93Thr
ENST00000644683.1:c.277C>A ENSP00000494085.1:p.Pro93Thr
ENST00000644810.1:c.230-576C>A ENSP00000495895.1:n.230-576C>A
ENST00000644831.1:n.306C>A
ENST00000644933.1:c.-453C>A ENSP00000496133.1:n.-453C>A
ENST00000645020.1:n.1305C>A
ENST00000645285.1:c.-453C>A ENSP00000495058.1:n.-453C>A
ENST00000645331.1:n.299C>A
ENST00000645620.1:c.-395C>A ENSP00000493657.1:n.-395C>A
ENST00000646777.1:n.306C>A
ENST00000647016.1:n.610C>A
ENST00000647152.1:c.-453C>A ENSP00000495893.1:n.-453C>A
ENST00000647209.1:c.*146C>A ENSP00000495558.1:n.*146C>A
ENST00000647346.1:n.1297C>A
ENST00000299427.10:c.277C>A ENSP00000299427.6:p.Pro93Thr
ENST00000428886.6:n.299C>A
ENST00000436873.6:c.277C>A ENSP00000398136.2:p.Pro93Thr
ENST00000528571.5:c.*17C>A ENSP00000434647.1:n.*17C>A
ENST00000530040.1:n.389C>A
ENST00000533371.5:c.-453C>A ENSP00000437066.1:n.-453C>A
ENST00000534644.5:n.262C>A
ENST00000611494.4:c.277C>A ENSP00000484546.1:p.Pro93Thr
NM_000391.3:c.277C>A NP_000382.3:p.Pro93Thr
NM_000391.4:c.277C>A MANE Select NP_000382.3:p.Pro93Thr