Canonical Allele Identifier: CA1950215563
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6618017C= , CM000673.2:g.6618017C= GRCh38
NC_000011.9:g.6639248C= , CM000673.1:g.6639248C= GRCh37
NC_000011.8:g.6595824C= NCBI36
NG_008653.1:g.6445G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-241G= ENSP00000507321.1:n.116-241G=
ENST00000299427.12:c.230-241G= MANE Select ENSP00000299427.6:n.230-241G=
ENST00000428886.7:n.318-241G=
ENST00000436873.7:c.34-241G=
ENST00000524788.2:n.1001G=
ENST00000524903.2:n.1117G=
ENST00000528571.6:c.90-241G= ENSP00000434647.1:n.90-241G=
ENST00000530040.2:n.259-241G=
ENST00000533371.6:c.-500-241G= ENSP00000437066.1:n.-500-241G=
ENST00000534644.6:n.231-241G=
ENST00000642892.1:c.-447-241G= ENSP00000494165.1:n.-447-241G=
ENST00000643439.1:c.90-241G= ENSP00000495849.1:n.90-241G=
ENST00000643479.1:n.259-241G=
ENST00000643516.1:c.117-241G=
ENST00000644151.1:n.1281G=
ENST00000644218.1:c.230-241G= ENSP00000493574.1:n.230-241G=
ENST00000644683.1:c.230-241G= ENSP00000494085.1:n.230-241G=
ENST00000644810.1:c.229+759G= ENSP00000495895.1:n.229+759G=
ENST00000644831.1:n.259-241G=
ENST00000644933.1:c.-500-241G= ENSP00000496133.1:n.-500-241G=
ENST00000645020.1:n.1017G=
ENST00000645285.1:c.-500-241G= ENSP00000495058.1:n.-500-241G=
ENST00000645331.1:n.252-241G=
ENST00000645620.1:c.-442-241G= ENSP00000493657.1:n.-442-241G=
ENST00000646777.1:n.259-241G=
ENST00000647016.1:n.322G=
ENST00000647152.1:c.-500-241G= ENSP00000495893.1:n.-500-241G=
ENST00000647209.1:c.*99-241G= ENSP00000495558.1:n.*99-241G=
ENST00000647346.1:n.1009G=
ENST00000299427.10:c.230-241G= ENSP00000299427.6:n.230-241G=
ENST00000428886.6:n.252-241G=
ENST00000436873.6:c.230-241G= ENSP00000398136.2:n.230-241G=
ENST00000528571.5:c.90-241G= ENSP00000434647.1:n.90-241G=
ENST00000528917.1:n.531-241G=
ENST00000530040.1:n.342-241G=
ENST00000533371.5:c.-500-241G= ENSP00000437066.1:n.-500-241G=
ENST00000534644.5:n.215-241G=
ENST00000611494.4:c.230-241G= ENSP00000484546.1:n.230-241G=
NM_000391.3:c.230-241G= NP_000382.3:n.230-241G=
NM_000391.4:c.230-241G= MANE Select NP_000382.3:n.230-241G=