Canonical Allele Identifier: CA1950215464
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617845A= , CM000673.2:g.6617845A= GRCh38
NC_000011.9:g.6639076A= , CM000673.1:g.6639076A= GRCh37
NC_000011.8:g.6595652A= NCBI36
NG_008653.1:g.6617T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-69T= ENSP00000507321.1:n.116-69T=
ENST00000299427.12:c.230-69T= MANE Select ENSP00000299427.6:n.230-69T=
ENST00000428886.7:n.318-69T=
ENST00000436873.7:c.34-69T=
ENST00000524788.2:n.1173T=
ENST00000524903.2:n.1289T=
ENST00000528571.6:c.90-69T= ENSP00000434647.1:n.90-69T=
ENST00000530040.2:n.259-69T=
ENST00000533371.6:c.-500-69T= ENSP00000437066.1:n.-500-69T=
ENST00000534644.6:n.231-69T=
ENST00000642892.1:c.-447-69T= ENSP00000494165.1:n.-447-69T=
ENST00000643439.1:c.90-69T= ENSP00000495849.1:n.90-69T=
ENST00000643479.1:n.259-69T=
ENST00000643516.1:c.117-69T=
ENST00000644151.1:n.1453T=
ENST00000644218.1:c.230-69T= ENSP00000493574.1:n.230-69T=
ENST00000644683.1:c.230-69T= ENSP00000494085.1:n.230-69T=
ENST00000644810.1:c.230-692T= ENSP00000495895.1:n.230-692T=
ENST00000644831.1:n.259-69T=
ENST00000644933.1:c.-500-69T= ENSP00000496133.1:n.-500-69T=
ENST00000645020.1:n.1189T=
ENST00000645285.1:c.-500-69T= ENSP00000495058.1:n.-500-69T=
ENST00000645331.1:n.252-69T=
ENST00000645620.1:c.-442-69T= ENSP00000493657.1:n.-442-69T=
ENST00000646777.1:n.259-69T=
ENST00000647016.1:n.494T=
ENST00000647152.1:c.-500-69T= ENSP00000495893.1:n.-500-69T=
ENST00000647209.1:c.*99-69T= ENSP00000495558.1:n.*99-69T=
ENST00000647346.1:n.1181T=
ENST00000299427.10:c.230-69T= ENSP00000299427.6:n.230-69T=
ENST00000428886.6:n.252-69T=
ENST00000436873.6:c.230-69T= ENSP00000398136.2:n.230-69T=
ENST00000528571.5:c.90-69T= ENSP00000434647.1:n.90-69T=
ENST00000528917.1:n.531-69T=
ENST00000530040.1:n.342-69T=
ENST00000533371.5:c.-500-69T= ENSP00000437066.1:n.-500-69T=
ENST00000534644.5:n.215-69T=
ENST00000611494.4:c.230-69T= ENSP00000484546.1:n.230-69T=
NM_000391.3:c.230-69T= NP_000382.3:n.230-69T=
NM_000391.4:c.230-69T= MANE Select NP_000382.3:n.230-69T=