Canonical Allele Identifier: CA1950215251
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617672G= , CM000673.2:g.6617672G= GRCh38
NC_000011.9:g.6638903G= , CM000673.1:g.6638903G= GRCh37
NC_000011.8:g.6595479G= NCBI36
NG_008653.1:g.6790C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.220C= ENSP00000507321.1:p.His74=
ENST00000299427.12:c.334C= MANE Select ENSP00000299427.6:p.His112=
ENST00000428886.7:n.422C=
ENST00000436873.7:c.138C=
ENST00000524788.2:n.1346C=
ENST00000524903.2:n.1462C=
ENST00000528571.6:c.*74C= ENSP00000434647.1:n.*74C=
ENST00000530040.2:n.363C=
ENST00000533371.6:c.-396C= ENSP00000437066.1:n.-396C=
ENST00000534644.6:n.335C=
ENST00000642892.1:c.-343C= ENSP00000494165.1:n.-343C=
ENST00000643439.1:c.*74C= ENSP00000495849.1:n.*74C=
ENST00000643479.1:n.363C=
ENST00000643516.1:c.221C=
ENST00000644151.1:n.1626C=
ENST00000644218.1:c.334C= ENSP00000493574.1:p.His112=
ENST00000644683.1:c.334C= ENSP00000494085.1:p.His112=
ENST00000644810.1:c.230-519C= ENSP00000495895.1:n.230-519C=
ENST00000644831.1:n.363C=
ENST00000644933.1:c.-396C= ENSP00000496133.1:n.-396C=
ENST00000645020.1:n.1362C=
ENST00000645285.1:c.-396C= ENSP00000495058.1:n.-396C=
ENST00000645331.1:n.356C=
ENST00000645620.1:c.-338C= ENSP00000493657.1:n.-338C=
ENST00000646777.1:n.363C=
ENST00000647016.1:n.667C=
ENST00000647152.1:c.-396C= ENSP00000495893.1:n.-396C=
ENST00000647209.1:c.*203C= ENSP00000495558.1:n.*203C=
ENST00000647346.1:n.1354C=
ENST00000299427.10:c.334C= ENSP00000299427.6:p.His112=
ENST00000428886.6:n.356C=
ENST00000436873.6:c.334C= ENSP00000398136.2:p.His112=
ENST00000528571.5:c.*74C= ENSP00000434647.1:n.*74C=
ENST00000530040.1:n.446C=
ENST00000533371.5:c.-396C= ENSP00000437066.1:n.-396C=
ENST00000534644.5:n.319C=
ENST00000611494.4:c.334C= ENSP00000484546.1:p.His112=
NM_000391.3:c.334C= NP_000382.3:p.His112=
NM_000391.4:c.334C= MANE Select NP_000382.3:p.His112=