Canonical Allele Identifier: CA1950237247
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616736T= , CM000673.2:g.6616736T= GRCh38
NC_000011.9:g.6637967T= , CM000673.1:g.6637967T= GRCh37
NC_000011.8:g.6594543T= NCBI36
NG_008653.1:g.7726A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.697A= ENSP00000507321.1:p.Ile233=
ENST00000299427.12:c.811A= MANE Select ENSP00000299427.6:p.Ile271=
ENST00000436873.7:c.312+565A=
ENST00000524788.2:n.1970A=
ENST00000524903.2:n.2086A=
ENST00000528807.2:n.467A=
ENST00000530040.2:n.480-233A=
ENST00000533371.6:c.82A= ENSP00000437066.1:p.Ile28=
ENST00000642892.1:c.82A= ENSP00000494165.1:p.Ile28=
ENST00000643439.1:c.*551A= ENSP00000495849.1:n.*551A=
ENST00000643479.1:n.840A=
ENST00000643516.1:c.396-233A=
ENST00000644151.1:n.2250A=
ENST00000644218.1:c.811A= ENSP00000493574.1:p.Ile271=
ENST00000644683.1:c.*264A= ENSP00000494085.1:n.*264A=
ENST00000644810.1:c.532A= ENSP00000495895.1:p.Ile178=
ENST00000644831.1:n.987A=
ENST00000644933.1:c.82A= ENSP00000496133.1:p.Ile28=
ENST00000645020.1:n.2101A=
ENST00000645285.1:c.82A= ENSP00000495058.1:p.Ile28=
ENST00000645331.1:n.1177A=
ENST00000645620.1:c.82A= ENSP00000493657.1:p.Ile28=
ENST00000646777.1:n.987A=
ENST00000647016.1:n.1291A=
ENST00000647152.1:c.82A= ENSP00000495893.1:p.Ile28=
ENST00000647209.1:c.*680A= ENSP00000495558.1:n.*680A=
ENST00000647346.1:n.1831A=
ENST00000299427.10:c.811A= ENSP00000299427.6:p.Ile271=
ENST00000436873.6:c.451-233A= ENSP00000398136.2:n.451-233A=
ENST00000524788.1:n.511A=
ENST00000528807.1:n.361A=
ENST00000533371.5:c.82A= ENSP00000437066.1:p.Ile28=
ENST00000611494.4:c.811A= ENSP00000484546.1:p.Ile271=
NM_000391.3:c.811A= NP_000382.3:p.Ile271=
NM_000391.4:c.811A= MANE Select NP_000382.3:p.Ile271=