Canonical Allele Identifier: CA1950237135
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616684G= , CM000673.2:g.6616684G= GRCh38
NC_000011.9:g.6637915G= , CM000673.1:g.6637915G= GRCh37
NC_000011.8:g.6594491G= NCBI36
NG_008653.1:g.7778C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.749C= ENSP00000507321.1:p.Ser250=
ENST00000299427.12:c.863C= MANE Select ENSP00000299427.6:p.Ser288=
ENST00000436873.7:c.313-610C=
ENST00000524788.2:n.2022C=
ENST00000524903.2:n.2138C=
ENST00000528807.2:n.519C=
ENST00000530040.2:n.480-181C=
ENST00000533371.6:c.134C= ENSP00000437066.1:p.Ser45=
ENST00000642892.1:c.134C= ENSP00000494165.1:p.Ser45=
ENST00000643439.1:c.*603C= ENSP00000495849.1:n.*603C=
ENST00000643479.1:n.892C=
ENST00000643516.1:c.396-181C=
ENST00000644151.1:n.2302C=
ENST00000644218.1:c.863C= ENSP00000493574.1:p.Ser288=
ENST00000644683.1:c.*316C= ENSP00000494085.1:n.*316C=
ENST00000644810.1:c.584C= ENSP00000495895.1:p.Ser195=
ENST00000644831.1:n.1039C=
ENST00000644933.1:c.134C= ENSP00000496133.1:p.Ser45=
ENST00000645020.1:n.2153C=
ENST00000645285.1:c.134C= ENSP00000495058.1:p.Ser45=
ENST00000645331.1:n.1229C=
ENST00000645620.1:c.134C= ENSP00000493657.1:p.Ser45=
ENST00000646777.1:n.1039C=
ENST00000647016.1:n.1343C=
ENST00000647152.1:c.134C= ENSP00000495893.1:p.Ser45=
ENST00000647209.1:c.*732C= ENSP00000495558.1:n.*732C=
ENST00000647346.1:n.1883C=
ENST00000299427.10:c.863C= ENSP00000299427.6:p.Ser288=
ENST00000436873.6:c.451-181C= ENSP00000398136.2:n.451-181C=
ENST00000528807.1:n.413C=
ENST00000533371.5:c.134C= ENSP00000437066.1:p.Ser45=
ENST00000611494.4:c.863C= ENSP00000484546.1:p.Ser288=
NM_000391.3:c.863C= NP_000382.3:p.Ser288=
NM_000391.4:c.863C= MANE Select NP_000382.3:p.Ser288=