Canonical Allele Identifier: CA472922981
Gene: TPP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.6638590A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617359A>T , CM000673.2:g.6617359A>T GRCh38
NC_000011.9:g.6638590A>T , CM000673.1:g.6638590A>T GRCh37
NC_000011.8:g.6595166A>T NCBI36
NG_008653.1:g.7103T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.336T>A ENSP00000507321.1:p.Val112=
ENST00000299427.12:c.450T>A MANE Select ENSP00000299427.6:p.Val150=
ENST00000428886.7:n.538T>A
ENST00000436873.7:c.254T>A
ENST00000524788.2:n.1462T>A
ENST00000524903.2:n.1578T>A
ENST00000528571.6:c.*190T>A ENSP00000434647.1:n.*190T>A
ENST00000528807.2:n.106T>A
ENST00000530040.2:n.479T>A
ENST00000533371.6:c.-280T>A ENSP00000437066.1:n.-280T>A
ENST00000534644.6:n.451T>A
ENST00000642892.1:c.-227T>A ENSP00000494165.1:n.-227T>A
ENST00000643439.1:c.*190T>A ENSP00000495849.1:n.*190T>A
ENST00000643479.1:n.479T>A
ENST00000643516.1:c.337T>A
ENST00000644151.1:n.1742T>A
ENST00000644218.1:c.450T>A ENSP00000493574.1:p.Val150=
ENST00000644683.1:c.450T>A ENSP00000494085.1:p.Val150=
ENST00000644810.1:c.230-206T>A ENSP00000495895.1:n.230-206T>A
ENST00000644831.1:n.479T>A
ENST00000644933.1:c.-280T>A ENSP00000496133.1:n.-280T>A
ENST00000645020.1:n.1478T>A
ENST00000645285.1:c.-280T>A ENSP00000495058.1:n.-280T>A
ENST00000645331.1:n.669T>A
ENST00000645620.1:c.-222T>A ENSP00000493657.1:n.-222T>A
ENST00000646777.1:n.479T>A
ENST00000647016.1:n.783T>A
ENST00000647152.1:c.-280T>A ENSP00000495893.1:n.-280T>A
ENST00000647209.1:c.*319T>A ENSP00000495558.1:n.*319T>A
ENST00000647346.1:n.1470T>A
ENST00000299427.10:c.450T>A ENSP00000299427.6:p.Val150=
ENST00000428886.6:n.472T>A
ENST00000436873.6:c.450T>A ENSP00000398136.2:p.Val150=
ENST00000524788.1:n.3T>A
ENST00000528571.5:c.*190T>A ENSP00000434647.1:n.*190T>A
ENST00000533371.5:c.-280T>A ENSP00000437066.1:n.-280T>A
ENST00000534644.5:n.435T>A
ENST00000611494.4:c.450T>A ENSP00000484546.1:p.Val150=
NM_000391.3:c.450T>A NP_000382.3:p.Val150=
NM_000391.4:c.450T>A MANE Select NP_000382.3:p.Val150=