Canonical Allele Identifier: CA379475559
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617100G>T , CM000673.2:g.6617100G>T GRCh38
NC_000011.9:g.6638331G>T , CM000673.1:g.6638331G>T GRCh37
NC_000011.8:g.6594907G>T NCBI36
NG_008653.1:g.7362C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.448C>A ENSP00000507321.1:p.Pro150Thr
ENST00000299427.12:c.562C>A MANE Select ENSP00000299427.6:p.Pro188Thr
ENST00000428886.7:n.797C>A
ENST00000436873.7:c.312+201C>A
ENST00000524788.2:n.1721C>A
ENST00000524903.2:n.1837C>A
ENST00000528807.2:n.218C>A
ENST00000530040.2:n.479+259C>A
ENST00000533371.6:c.-168C>A ENSP00000437066.1:n.-168C>A
ENST00000534644.6:n.510C>A
ENST00000642892.1:c.-168C>A ENSP00000494165.1:n.-168C>A
ENST00000643439.1:c.*302C>A ENSP00000495849.1:n.*302C>A
ENST00000643479.1:n.591C>A
ENST00000643516.1:c.395+201C>A
ENST00000644151.1:n.2001C>A
ENST00000644218.1:c.562C>A ENSP00000493574.1:p.Pro188Thr
ENST00000644683.1:c.*15C>A ENSP00000494085.1:n.*15C>A
ENST00000644810.1:c.283C>A ENSP00000495895.1:p.Pro95Thr
ENST00000644831.1:n.738C>A
ENST00000644933.1:c.-168C>A ENSP00000496133.1:n.-168C>A
ENST00000645020.1:n.1737C>A
ENST00000645285.1:c.-168C>A ENSP00000495058.1:n.-168C>A
ENST00000645331.1:n.928C>A
ENST00000645620.1:c.-168C>A ENSP00000493657.1:n.-168C>A
ENST00000646777.1:n.738C>A
ENST00000647016.1:n.1042C>A
ENST00000647152.1:c.-168C>A ENSP00000495893.1:n.-168C>A
ENST00000647209.1:c.*431C>A ENSP00000495558.1:n.*431C>A
ENST00000647346.1:n.1582C>A
ENST00000299427.10:c.562C>A ENSP00000299427.6:p.Pro188Thr
ENST00000428886.6:n.731C>A
ENST00000436873.6:c.450+259C>A ENSP00000398136.2:n.450+259C>A
ENST00000524788.1:n.262C>A
ENST00000528571.5:c.*302C>A ENSP00000434647.1:n.*302C>A
ENST00000528807.1:n.112C>A
ENST00000533371.5:c.-168C>A ENSP00000437066.1:n.-168C>A
ENST00000534644.5:n.547C>A
ENST00000611494.4:c.562C>A ENSP00000484546.1:p.Pro188Thr
NM_000391.3:c.562C>A NP_000382.3:p.Pro188Thr
NM_000391.4:c.562C>A MANE Select NP_000382.3:p.Pro188Thr