Canonical Allele Identifier: CA379475427
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617034T>A , CM000673.2:g.6617034T>A GRCh38
NC_000011.9:g.6638265T>A , CM000673.1:g.6638265T>A GRCh37
NC_000011.8:g.6594841T>A NCBI36
NG_008653.1:g.7428A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.514A>T ENSP00000507321.1:p.Asn172Tyr
ENST00000299427.12:c.628A>T MANE Select ENSP00000299427.6:p.Asn210Tyr
ENST00000436873.7:c.312+267A>T
ENST00000524788.2:n.1787A>T
ENST00000524903.2:n.1903A>T
ENST00000528807.2:n.284A>T
ENST00000530040.2:n.479+325A>T
ENST00000533371.6:c.-102A>T ENSP00000437066.1:n.-102A>T
ENST00000534644.6:n.576A>T
ENST00000642892.1:c.-102A>T ENSP00000494165.1:n.-102A>T
ENST00000643439.1:c.*368A>T ENSP00000495849.1:n.*368A>T
ENST00000643479.1:n.657A>T
ENST00000643516.1:c.395+267A>T
ENST00000644151.1:n.2067A>T
ENST00000644218.1:c.628A>T ENSP00000493574.1:p.Asn210Tyr
ENST00000644683.1:c.*81A>T ENSP00000494085.1:n.*81A>T
ENST00000644810.1:c.349A>T ENSP00000495895.1:p.Asn117Tyr
ENST00000644831.1:n.804A>T
ENST00000644933.1:c.-102A>T ENSP00000496133.1:n.-102A>T
ENST00000645020.1:n.1803A>T
ENST00000645285.1:c.-102A>T ENSP00000495058.1:n.-102A>T
ENST00000645331.1:n.994A>T
ENST00000645620.1:c.-102A>T ENSP00000493657.1:n.-102A>T
ENST00000646777.1:n.804A>T
ENST00000647016.1:n.1108A>T
ENST00000647152.1:c.-102A>T ENSP00000495893.1:n.-102A>T
ENST00000647209.1:c.*497A>T ENSP00000495558.1:n.*497A>T
ENST00000647346.1:n.1648A>T
ENST00000299427.10:c.628A>T ENSP00000299427.6:p.Asn210Tyr
ENST00000428886.6:n.797A>T
ENST00000436873.6:c.450+325A>T ENSP00000398136.2:n.450+325A>T
ENST00000524788.1:n.328A>T
ENST00000528571.5:c.*368A>T ENSP00000434647.1:n.*368A>T
ENST00000528807.1:n.178A>T
ENST00000533371.5:c.-102A>T ENSP00000437066.1:n.-102A>T
ENST00000534644.5:n.613A>T
ENST00000611494.4:c.628A>T ENSP00000484546.1:p.Asn210Tyr
NM_000391.3:c.628A>T NP_000382.3:p.Asn210Tyr
NM_000391.4:c.628A>T MANE Select NP_000382.3:p.Asn210Tyr