Canonical Allele Identifier: CA379475532
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617087C>T , CM000673.2:g.6617087C>T GRCh38
NC_000011.9:g.6638318C>T , CM000673.1:g.6638318C>T GRCh37
NC_000011.8:g.6594894C>T NCBI36
NG_008653.1:g.7375G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.461G>A ENSP00000507321.1:p.Gly154Glu
ENST00000299427.12:c.575G>A MANE Select ENSP00000299427.6:p.Gly192Glu
ENST00000428886.7:n.810G>A
ENST00000436873.7:c.312+214G>A
ENST00000524788.2:n.1734G>A
ENST00000524903.2:n.1850G>A
ENST00000528807.2:n.231G>A
ENST00000530040.2:n.479+272G>A
ENST00000533371.6:c.-155G>A ENSP00000437066.1:n.-155G>A
ENST00000534644.6:n.523G>A
ENST00000642892.1:c.-155G>A ENSP00000494165.1:n.-155G>A
ENST00000643439.1:c.*315G>A ENSP00000495849.1:n.*315G>A
ENST00000643479.1:n.604G>A
ENST00000643516.1:c.395+214G>A
ENST00000644151.1:n.2014G>A
ENST00000644218.1:c.575G>A ENSP00000493574.1:p.Gly192Glu
ENST00000644683.1:c.*28G>A ENSP00000494085.1:n.*28G>A
ENST00000644810.1:c.296G>A ENSP00000495895.1:p.Gly99Glu
ENST00000644831.1:n.751G>A
ENST00000644933.1:c.-155G>A ENSP00000496133.1:n.-155G>A
ENST00000645020.1:n.1750G>A
ENST00000645285.1:c.-155G>A ENSP00000495058.1:n.-155G>A
ENST00000645331.1:n.941G>A
ENST00000645620.1:c.-155G>A ENSP00000493657.1:n.-155G>A
ENST00000646777.1:n.751G>A
ENST00000647016.1:n.1055G>A
ENST00000647152.1:c.-155G>A ENSP00000495893.1:n.-155G>A
ENST00000647209.1:c.*444G>A ENSP00000495558.1:n.*444G>A
ENST00000647346.1:n.1595G>A
ENST00000299427.10:c.575G>A ENSP00000299427.6:p.Gly192Glu
ENST00000428886.6:n.744G>A
ENST00000436873.6:c.450+272G>A ENSP00000398136.2:n.450+272G>A
ENST00000524788.1:n.275G>A
ENST00000528571.5:c.*315G>A ENSP00000434647.1:n.*315G>A
ENST00000528807.1:n.125G>A
ENST00000533371.5:c.-155G>A ENSP00000437066.1:n.-155G>A
ENST00000534644.5:n.560G>A
ENST00000611494.4:c.575G>A ENSP00000484546.1:p.Gly192Glu
NM_000391.3:c.575G>A NP_000382.3:p.Gly192Glu
NM_000391.4:c.575G>A MANE Select NP_000382.3:p.Gly192Glu