Canonical Allele Identifier: CA1950237303
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616766C= , CM000673.2:g.6616766C= GRCh38
NC_000011.9:g.6637997C= , CM000673.1:g.6637997C= GRCh37
NC_000011.8:g.6594573C= NCBI36
NG_008653.1:g.7696G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.667G= ENSP00000507321.1:p.Val223=
ENST00000299427.12:c.781G= MANE Select ENSP00000299427.6:p.Val261=
ENST00000436873.7:c.312+535G=
ENST00000524788.2:n.1940G=
ENST00000524903.2:n.2056G=
ENST00000528807.2:n.437G=
ENST00000530040.2:n.480-263G=
ENST00000533371.6:c.52G= ENSP00000437066.1:p.Val18=
ENST00000642892.1:c.52G= ENSP00000494165.1:p.Val18=
ENST00000643439.1:c.*521G= ENSP00000495849.1:n.*521G=
ENST00000643479.1:n.810G=
ENST00000643516.1:c.396-263G=
ENST00000644151.1:n.2220G=
ENST00000644218.1:c.781G= ENSP00000493574.1:p.Val261=
ENST00000644683.1:c.*234G= ENSP00000494085.1:n.*234G=
ENST00000644810.1:c.502G= ENSP00000495895.1:p.Val168=
ENST00000644831.1:n.957G=
ENST00000644933.1:c.52G= ENSP00000496133.1:p.Val18=
ENST00000645020.1:n.2071G=
ENST00000645285.1:c.52G= ENSP00000495058.1:p.Val18=
ENST00000645331.1:n.1147G=
ENST00000645620.1:c.52G= ENSP00000493657.1:p.Val18=
ENST00000646777.1:n.957G=
ENST00000647016.1:n.1261G=
ENST00000647152.1:c.52G= ENSP00000495893.1:p.Val18=
ENST00000647209.1:c.*650G= ENSP00000495558.1:n.*650G=
ENST00000647346.1:n.1801G=
ENST00000299427.10:c.781G= ENSP00000299427.6:p.Val261=
ENST00000436873.6:c.451-263G= ENSP00000398136.2:n.451-263G=
ENST00000524788.1:n.481G=
ENST00000528807.1:n.331G=
ENST00000533371.5:c.52G= ENSP00000437066.1:p.Val18=
ENST00000611494.4:c.781G= ENSP00000484546.1:p.Val261=
NM_000391.3:c.781G= NP_000382.3:p.Val261=
NM_000391.4:c.781G= MANE Select NP_000382.3:p.Val261=