Canonical Allele Identifier: CA1950215296
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617695A= , CM000673.2:g.6617695A= GRCh38
NC_000011.9:g.6638926A= , CM000673.1:g.6638926A= GRCh37
NC_000011.8:g.6595502A= NCBI36
NG_008653.1:g.6767T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.197T= ENSP00000507321.1:p.Leu66=
ENST00000299427.12:c.311T= MANE Select ENSP00000299427.6:p.Leu104=
ENST00000428886.7:n.399T=
ENST00000436873.7:c.115T=
ENST00000524788.2:n.1323T=
ENST00000524903.2:n.1439T=
ENST00000528571.6:c.*51T= ENSP00000434647.1:n.*51T=
ENST00000530040.2:n.340T=
ENST00000533371.6:c.-419T= ENSP00000437066.1:n.-419T=
ENST00000534644.6:n.312T=
ENST00000642892.1:c.-366T= ENSP00000494165.1:n.-366T=
ENST00000643439.1:c.*51T= ENSP00000495849.1:n.*51T=
ENST00000643479.1:n.340T=
ENST00000643516.1:c.198T=
ENST00000644151.1:n.1603T=
ENST00000644218.1:c.311T= ENSP00000493574.1:p.Leu104=
ENST00000644683.1:c.311T= ENSP00000494085.1:p.Leu104=
ENST00000644810.1:c.230-542T= ENSP00000495895.1:n.230-542T=
ENST00000644831.1:n.340T=
ENST00000644933.1:c.-419T= ENSP00000496133.1:n.-419T=
ENST00000645020.1:n.1339T=
ENST00000645285.1:c.-419T= ENSP00000495058.1:n.-419T=
ENST00000645331.1:n.333T=
ENST00000645620.1:c.-361T= ENSP00000493657.1:n.-361T=
ENST00000646777.1:n.340T=
ENST00000647016.1:n.644T=
ENST00000647152.1:c.-419T= ENSP00000495893.1:n.-419T=
ENST00000647209.1:c.*180T= ENSP00000495558.1:n.*180T=
ENST00000647346.1:n.1331T=
ENST00000299427.10:c.311T= ENSP00000299427.6:p.Leu104=
ENST00000428886.6:n.333T=
ENST00000436873.6:c.311T= ENSP00000398136.2:p.Leu104=
ENST00000528571.5:c.*51T= ENSP00000434647.1:n.*51T=
ENST00000530040.1:n.423T=
ENST00000533371.5:c.-419T= ENSP00000437066.1:n.-419T=
ENST00000534644.5:n.296T=
ENST00000611494.4:c.311T= ENSP00000484546.1:p.Leu104=
NM_000391.3:c.311T= NP_000382.3:p.Leu104=
NM_000391.4:c.311T= MANE Select NP_000382.3:p.Leu104=