Canonical Allele Identifier: CA379475105
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616781A>T , CM000673.2:g.6616781A>T GRCh38
NC_000011.9:g.6638012A>T , CM000673.1:g.6638012A>T GRCh37
NC_000011.8:g.6594588A>T NCBI36
NG_008653.1:g.7681T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.652T>A ENSP00000507321.1:p.Ser218Thr
ENST00000299427.12:c.766T>A MANE Select ENSP00000299427.6:p.Ser256Thr
ENST00000436873.7:c.312+520T>A
ENST00000524788.2:n.1925T>A
ENST00000524903.2:n.2041T>A
ENST00000528807.2:n.422T>A
ENST00000530040.2:n.480-278T>A
ENST00000533371.6:c.37T>A ENSP00000437066.1:p.Ser13Thr
ENST00000642892.1:c.37T>A ENSP00000494165.1:p.Ser13Thr
ENST00000643439.1:c.*506T>A ENSP00000495849.1:n.*506T>A
ENST00000643479.1:n.795T>A
ENST00000643516.1:c.396-278T>A
ENST00000644151.1:n.2205T>A
ENST00000644218.1:c.766T>A ENSP00000493574.1:p.Ser256Thr
ENST00000644683.1:c.*219T>A ENSP00000494085.1:n.*219T>A
ENST00000644810.1:c.487T>A ENSP00000495895.1:p.Ser163Thr
ENST00000644831.1:n.942T>A
ENST00000644933.1:c.37T>A ENSP00000496133.1:p.Ser13Thr
ENST00000645020.1:n.2056T>A
ENST00000645285.1:c.37T>A ENSP00000495058.1:p.Ser13Thr
ENST00000645331.1:n.1132T>A
ENST00000645620.1:c.37T>A ENSP00000493657.1:p.Ser13Thr
ENST00000646777.1:n.942T>A
ENST00000647016.1:n.1246T>A
ENST00000647152.1:c.37T>A ENSP00000495893.1:p.Ser13Thr
ENST00000647209.1:c.*635T>A ENSP00000495558.1:n.*635T>A
ENST00000647346.1:n.1786T>A
ENST00000299427.10:c.766T>A ENSP00000299427.6:p.Ser256Thr
ENST00000436873.6:c.451-278T>A ENSP00000398136.2:n.451-278T>A
ENST00000524788.1:n.466T>A
ENST00000528807.1:n.316T>A
ENST00000533371.5:c.37T>A ENSP00000437066.1:p.Ser13Thr
ENST00000611494.4:c.766T>A ENSP00000484546.1:p.Ser256Thr
NM_000391.3:c.766T>A NP_000382.3:p.Ser256Thr
NM_000391.4:c.766T>A MANE Select NP_000382.3:p.Ser256Thr