Canonical Allele Identifier: CA1950237200
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616714T= , CM000673.2:g.6616714T= GRCh38
NC_000011.9:g.6637945T= , CM000673.1:g.6637945T= GRCh37
NC_000011.8:g.6594521T= NCBI36
NG_008653.1:g.7748A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.719A= ENSP00000507321.1:p.Gln240=
ENST00000299427.12:c.833A= MANE Select ENSP00000299427.6:p.Gln278=
ENST00000436873.7:c.312+587A=
ENST00000524788.2:n.1992A=
ENST00000524903.2:n.2108A=
ENST00000528807.2:n.489A=
ENST00000530040.2:n.480-211A=
ENST00000533371.6:c.104A= ENSP00000437066.1:p.Gln35=
ENST00000642892.1:c.104A= ENSP00000494165.1:p.Gln35=
ENST00000643439.1:c.*573A= ENSP00000495849.1:n.*573A=
ENST00000643479.1:n.862A=
ENST00000643516.1:c.396-211A=
ENST00000644151.1:n.2272A=
ENST00000644218.1:c.833A= ENSP00000493574.1:p.Gln278=
ENST00000644683.1:c.*286A= ENSP00000494085.1:n.*286A=
ENST00000644810.1:c.554A= ENSP00000495895.1:p.Gln185=
ENST00000644831.1:n.1009A=
ENST00000644933.1:c.104A= ENSP00000496133.1:p.Gln35=
ENST00000645020.1:n.2123A=
ENST00000645285.1:c.104A= ENSP00000495058.1:p.Gln35=
ENST00000645331.1:n.1199A=
ENST00000645620.1:c.104A= ENSP00000493657.1:p.Gln35=
ENST00000646777.1:n.1009A=
ENST00000647016.1:n.1313A=
ENST00000647152.1:c.104A= ENSP00000495893.1:p.Gln35=
ENST00000647209.1:c.*702A= ENSP00000495558.1:n.*702A=
ENST00000647346.1:n.1853A=
ENST00000299427.10:c.833A= ENSP00000299427.6:p.Gln278=
ENST00000436873.6:c.451-211A= ENSP00000398136.2:n.451-211A=
ENST00000524788.1:n.533A=
ENST00000528807.1:n.383A=
ENST00000533371.5:c.104A= ENSP00000437066.1:p.Gln35=
ENST00000611494.4:c.833A= ENSP00000484546.1:p.Gln278=
NM_000391.3:c.833A= NP_000382.3:p.Gln278=
NM_000391.4:c.833A= MANE Select NP_000382.3:p.Gln278=