Canonical Allele Identifier: CA1950215233
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617647A= , CM000673.2:g.6617647A= GRCh38
NC_000011.9:g.6638878A= , CM000673.1:g.6638878A= GRCh37
NC_000011.8:g.6595454A= NCBI36
NG_008653.1:g.6815T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.245T= ENSP00000507321.1:p.Leu82=
ENST00000299427.12:c.359T= MANE Select ENSP00000299427.6:p.Leu120=
ENST00000428886.7:n.447T=
ENST00000436873.7:c.163T=
ENST00000524788.2:n.1371T=
ENST00000524903.2:n.1487T=
ENST00000528571.6:c.*99T= ENSP00000434647.1:n.*99T=
ENST00000530040.2:n.388T=
ENST00000533371.6:c.-371T= ENSP00000437066.1:n.-371T=
ENST00000534644.6:n.360T=
ENST00000642892.1:c.-318T= ENSP00000494165.1:n.-318T=
ENST00000643439.1:c.*99T= ENSP00000495849.1:n.*99T=
ENST00000643479.1:n.388T=
ENST00000643516.1:c.246T=
ENST00000644151.1:n.1651T=
ENST00000644218.1:c.359T= ENSP00000493574.1:p.Leu120=
ENST00000644683.1:c.359T= ENSP00000494085.1:p.Leu120=
ENST00000644810.1:c.230-494T= ENSP00000495895.1:n.230-494T=
ENST00000644831.1:n.388T=
ENST00000644933.1:c.-371T= ENSP00000496133.1:n.-371T=
ENST00000645020.1:n.1387T=
ENST00000645285.1:c.-371T= ENSP00000495058.1:n.-371T=
ENST00000645331.1:n.381T=
ENST00000645620.1:c.-313T= ENSP00000493657.1:n.-313T=
ENST00000646777.1:n.388T=
ENST00000647016.1:n.692T=
ENST00000647152.1:c.-371T= ENSP00000495893.1:n.-371T=
ENST00000647209.1:c.*228T= ENSP00000495558.1:n.*228T=
ENST00000647346.1:n.1379T=
ENST00000299427.10:c.359T= ENSP00000299427.6:p.Leu120=
ENST00000428886.6:n.381T=
ENST00000436873.6:c.359T= ENSP00000398136.2:p.Leu120=
ENST00000528571.5:c.*99T= ENSP00000434647.1:n.*99T=
ENST00000530040.1:n.471T=
ENST00000533371.5:c.-371T= ENSP00000437066.1:n.-371T=
ENST00000534644.5:n.344T=
ENST00000611494.4:c.359T= ENSP00000484546.1:p.Leu120=
NM_000391.3:c.359T= NP_000382.3:p.Leu120=
NM_000391.4:c.359T= MANE Select NP_000382.3:p.Leu120=