Canonical Allele Identifier: CA2790314398
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617866_6617867insAGA , CM000673.2:g.6617866_6617867insAGA GRCh38
NC_000011.9:g.6639097_6639098insAGA , CM000673.1:g.6639097_6639098insAGA GRCh37
NC_000011.8:g.6595673_6595674insAGA NCBI36
NG_008653.1:g.6595_6596insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-91_116-90insTCT ENSP00000507321.1:n.116-91_116-90insTCT
ENST00000299427.12:c.230-91_230-90insTCT MANE Select ENSP00000299427.6:n.230-91_230-90insTCT
ENST00000428886.7:n.318-91_318-90insTCT
ENST00000436873.7:c.34-91_34-90insTCT
ENST00000524788.2:n.1151_1152insTCT
ENST00000524903.2:n.1267_1268insTCT
ENST00000528571.6:c.90-91_90-90insTCT ENSP00000434647.1:n.90-91_90-90insTCT
ENST00000530040.2:n.259-91_259-90insTCT
ENST00000533371.6:c.-500-91_-500-90insTCT ENSP00000437066.1:n.-500-91_-500-90insTCT
ENST00000534644.6:n.231-91_231-90insTCT
ENST00000642892.1:c.-447-91_-447-90insTCT ENSP00000494165.1:n.-447-91_-447-90insTCT
ENST00000643439.1:c.90-91_90-90insTCT ENSP00000495849.1:n.90-91_90-90insTCT
ENST00000643479.1:n.259-91_259-90insTCT
ENST00000643516.1:c.117-91_117-90insTCT
ENST00000644151.1:n.1431_1432insTCT
ENST00000644218.1:c.230-91_230-90insTCT ENSP00000493574.1:n.230-91_230-90insTCT
ENST00000644683.1:c.230-91_230-90insTCT ENSP00000494085.1:n.230-91_230-90insTCT
ENST00000644810.1:c.230-714_230-713insTCT ENSP00000495895.1:n.230-714_230-713insTCT
ENST00000644831.1:n.259-91_259-90insTCT
ENST00000644933.1:c.-500-91_-500-90insTCT ENSP00000496133.1:n.-500-91_-500-90insTCT
ENST00000645020.1:n.1167_1168insTCT
ENST00000645285.1:c.-500-91_-500-90insTCT ENSP00000495058.1:n.-500-91_-500-90insTCT
ENST00000645331.1:n.252-91_252-90insTCT
ENST00000645620.1:c.-442-91_-442-90insTCT ENSP00000493657.1:n.-442-91_-442-90insTCT
ENST00000646777.1:n.259-91_259-90insTCT
ENST00000647016.1:n.472_473insTCT
ENST00000647152.1:c.-500-91_-500-90insTCT ENSP00000495893.1:n.-500-91_-500-90insTCT
ENST00000647209.1:c.*99-91_*99-90insTCT ENSP00000495558.1:n.*99-91_*99-90insTCT
ENST00000647346.1:n.1159_1160insTCT
ENST00000299427.10:c.230-91_230-90insTCT ENSP00000299427.6:n.230-91_230-90insTCT
ENST00000428886.6:n.252-91_252-90insTCT
ENST00000436873.6:c.230-91_230-90insTCT ENSP00000398136.2:n.230-91_230-90insTCT
ENST00000528571.5:c.90-91_90-90insTCT ENSP00000434647.1:n.90-91_90-90insTCT
ENST00000528917.1:n.531-91_531-90insTCT
ENST00000530040.1:n.342-91_342-90insTCT
ENST00000533371.5:c.-500-91_-500-90insTCT ENSP00000437066.1:n.-500-91_-500-90insTCT
ENST00000534644.5:n.215-91_215-90insTCT
ENST00000611494.4:c.230-91_230-90insTCT ENSP00000484546.1:n.230-91_230-90insTCT
NM_000391.3:c.230-91_230-90insTCT NP_000382.3:n.230-91_230-90insTCT
NM_000391.4:c.230-91_230-90insTCT MANE Select NP_000382.3:n.230-91_230-90insTCT