Canonical Allele Identifier: CA379476186
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617645T>A , CM000673.2:g.6617645T>A GRCh38
NC_000011.9:g.6638876T>A , CM000673.1:g.6638876T>A GRCh37
NC_000011.8:g.6595452T>A NCBI36
NG_008653.1:g.6817A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.247A>T ENSP00000507321.1:p.Thr83Ser
ENST00000299427.12:c.361A>T MANE Select ENSP00000299427.6:p.Thr121Ser
ENST00000428886.7:n.449A>T
ENST00000436873.7:c.165A>T
ENST00000524788.2:n.1373A>T
ENST00000524903.2:n.1489A>T
ENST00000528571.6:c.*101A>T ENSP00000434647.1:n.*101A>T
ENST00000530040.2:n.390A>T
ENST00000533371.6:c.-369A>T ENSP00000437066.1:n.-369A>T
ENST00000534644.6:n.362A>T
ENST00000642892.1:c.-316A>T ENSP00000494165.1:n.-316A>T
ENST00000643439.1:c.*101A>T ENSP00000495849.1:n.*101A>T
ENST00000643479.1:n.390A>T
ENST00000643516.1:c.248A>T
ENST00000644151.1:n.1653A>T
ENST00000644218.1:c.361A>T ENSP00000493574.1:p.Thr121Ser
ENST00000644683.1:c.361A>T ENSP00000494085.1:p.Thr121Ser
ENST00000644810.1:c.230-492A>T ENSP00000495895.1:n.230-492A>T
ENST00000644831.1:n.390A>T
ENST00000644933.1:c.-369A>T ENSP00000496133.1:n.-369A>T
ENST00000645020.1:n.1389A>T
ENST00000645285.1:c.-369A>T ENSP00000495058.1:n.-369A>T
ENST00000645331.1:n.383A>T
ENST00000645620.1:c.-311A>T ENSP00000493657.1:n.-311A>T
ENST00000646777.1:n.390A>T
ENST00000647016.1:n.694A>T
ENST00000647152.1:c.-369A>T ENSP00000495893.1:n.-369A>T
ENST00000647209.1:c.*230A>T ENSP00000495558.1:n.*230A>T
ENST00000647346.1:n.1381A>T
ENST00000299427.10:c.361A>T ENSP00000299427.6:p.Thr121Ser
ENST00000428886.6:n.383A>T
ENST00000436873.6:c.361A>T ENSP00000398136.2:p.Thr121Ser
ENST00000528571.5:c.*101A>T ENSP00000434647.1:n.*101A>T
ENST00000530040.1:n.473A>T
ENST00000533371.5:c.-369A>T ENSP00000437066.1:n.-369A>T
ENST00000534644.5:n.346A>T
ENST00000611494.4:c.361A>T ENSP00000484546.1:p.Thr121Ser
NM_000391.3:c.361A>T NP_000382.3:p.Thr121Ser
NM_000391.4:c.361A>T MANE Select NP_000382.3:p.Thr121Ser