Canonical Allele Identifier: CA379476176
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617642A>T , CM000673.2:g.6617642A>T GRCh38
NC_000011.9:g.6638873A>T , CM000673.1:g.6638873A>T GRCh37
NC_000011.8:g.6595449A>T NCBI36
NG_008653.1:g.6820T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.250T>A ENSP00000507321.1:p.Cys84Ser
ENST00000299427.12:c.364T>A MANE Select ENSP00000299427.6:p.Cys122Ser
ENST00000428886.7:n.452T>A
ENST00000436873.7:c.168T>A
ENST00000524788.2:n.1376T>A
ENST00000524903.2:n.1492T>A
ENST00000528571.6:c.*104T>A ENSP00000434647.1:n.*104T>A
ENST00000530040.2:n.393T>A
ENST00000533371.6:c.-366T>A ENSP00000437066.1:n.-366T>A
ENST00000534644.6:n.365T>A
ENST00000642892.1:c.-313T>A ENSP00000494165.1:n.-313T>A
ENST00000643439.1:c.*104T>A ENSP00000495849.1:n.*104T>A
ENST00000643479.1:n.393T>A
ENST00000643516.1:c.251T>A
ENST00000644151.1:n.1656T>A
ENST00000644218.1:c.364T>A ENSP00000493574.1:p.Cys122Ser
ENST00000644683.1:c.364T>A ENSP00000494085.1:p.Cys122Ser
ENST00000644810.1:c.230-489T>A ENSP00000495895.1:n.230-489T>A
ENST00000644831.1:n.393T>A
ENST00000644933.1:c.-366T>A ENSP00000496133.1:n.-366T>A
ENST00000645020.1:n.1392T>A
ENST00000645285.1:c.-366T>A ENSP00000495058.1:n.-366T>A
ENST00000645331.1:n.386T>A
ENST00000645620.1:c.-308T>A ENSP00000493657.1:n.-308T>A
ENST00000646777.1:n.393T>A
ENST00000647016.1:n.697T>A
ENST00000647152.1:c.-366T>A ENSP00000495893.1:n.-366T>A
ENST00000647209.1:c.*233T>A ENSP00000495558.1:n.*233T>A
ENST00000647346.1:n.1384T>A
ENST00000299427.10:c.364T>A ENSP00000299427.6:p.Cys122Ser
ENST00000428886.6:n.386T>A
ENST00000436873.6:c.364T>A ENSP00000398136.2:p.Cys122Ser
ENST00000528571.5:c.*104T>A ENSP00000434647.1:n.*104T>A
ENST00000530040.1:n.476T>A
ENST00000533371.5:c.-366T>A ENSP00000437066.1:n.-366T>A
ENST00000534644.5:n.349T>A
ENST00000611494.4:c.364T>A ENSP00000484546.1:p.Cys122Ser
NM_000391.3:c.364T>A NP_000382.3:p.Cys122Ser
NM_000391.4:c.364T>A MANE Select NP_000382.3:p.Cys122Ser