Canonical Allele Identifier: CA1950215287
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617694C= , CM000673.2:g.6617694C= GRCh38
NC_000011.9:g.6638925C= , CM000673.1:g.6638925C= GRCh37
NC_000011.8:g.6595501C= NCBI36
NG_008653.1:g.6768G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.198G= ENSP00000507321.1:p.Leu66=
ENST00000299427.12:c.312G= MANE Select ENSP00000299427.6:p.Leu104=
ENST00000428886.7:n.400G=
ENST00000436873.7:c.116G=
ENST00000524788.2:n.1324G=
ENST00000524903.2:n.1440G=
ENST00000528571.6:c.*52G= ENSP00000434647.1:n.*52G=
ENST00000530040.2:n.341G=
ENST00000533371.6:c.-418G= ENSP00000437066.1:n.-418G=
ENST00000534644.6:n.313G=
ENST00000642892.1:c.-365G= ENSP00000494165.1:n.-365G=
ENST00000643439.1:c.*52G= ENSP00000495849.1:n.*52G=
ENST00000643479.1:n.341G=
ENST00000643516.1:c.199G=
ENST00000644151.1:n.1604G=
ENST00000644218.1:c.312G= ENSP00000493574.1:p.Leu104=
ENST00000644683.1:c.312G= ENSP00000494085.1:p.Leu104=
ENST00000644810.1:c.230-541G= ENSP00000495895.1:n.230-541G=
ENST00000644831.1:n.341G=
ENST00000644933.1:c.-418G= ENSP00000496133.1:n.-418G=
ENST00000645020.1:n.1340G=
ENST00000645285.1:c.-418G= ENSP00000495058.1:n.-418G=
ENST00000645331.1:n.334G=
ENST00000645620.1:c.-360G= ENSP00000493657.1:n.-360G=
ENST00000646777.1:n.341G=
ENST00000647016.1:n.645G=
ENST00000647152.1:c.-418G= ENSP00000495893.1:n.-418G=
ENST00000647209.1:c.*181G= ENSP00000495558.1:n.*181G=
ENST00000647346.1:n.1332G=
ENST00000299427.10:c.312G= ENSP00000299427.6:p.Leu104=
ENST00000428886.6:n.334G=
ENST00000436873.6:c.312G= ENSP00000398136.2:p.Leu104=
ENST00000528571.5:c.*52G= ENSP00000434647.1:n.*52G=
ENST00000530040.1:n.424G=
ENST00000533371.5:c.-418G= ENSP00000437066.1:n.-418G=
ENST00000534644.5:n.297G=
ENST00000611494.4:c.312G= ENSP00000484546.1:p.Leu104=
NM_000391.3:c.312G= NP_000382.3:p.Leu104=
NM_000391.4:c.312G= MANE Select NP_000382.3:p.Leu104=