Canonical Allele Identifier: CA1950215507
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617903_6617904delinsCA , CM000673.2:g.6617903_6617904delinsCA GRCh38
NC_000011.9:g.6639134_6639135delinsCA , CM000673.1:g.6639134_6639135delinsCA GRCh37
NC_000011.8:g.6595710_6595711delinsCA NCBI36
NG_008653.1:g.6558_6559delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-128_116-127delinsTG ENSP00000507321.1:n.116-128_116-127delinsTG
ENST00000299427.12:c.230-128_230-127delinsTG MANE Select ENSP00000299427.6:n.230-128_230-127delinsTG
ENST00000428886.7:n.318-128_318-127delinsTG
ENST00000436873.7:c.34-128_34-127delinsTG
ENST00000524788.2:n.1114_1115delinsTG
ENST00000524903.2:n.1230_1231delinsTG
ENST00000528571.6:c.90-128_90-127delinsTG ENSP00000434647.1:n.90-128_90-127delinsTG
ENST00000530040.2:n.259-128_259-127delinsTG
ENST00000533371.6:c.-500-128_-500-127delinsTG ENSP00000437066.1:n.-500-128_-500-127delinsTG
ENST00000534644.6:n.231-128_231-127delinsTG
ENST00000642892.1:c.-447-128_-447-127delinsTG ENSP00000494165.1:n.-447-128_-447-127delinsTG
ENST00000643439.1:c.90-128_90-127delinsTG ENSP00000495849.1:n.90-128_90-127delinsTG
ENST00000643479.1:n.259-128_259-127delinsTG
ENST00000643516.1:c.117-128_117-127delinsTG
ENST00000644151.1:n.1394_1395delinsTG
ENST00000644218.1:c.230-128_230-127delinsTG ENSP00000493574.1:n.230-128_230-127delinsTG
ENST00000644683.1:c.230-128_230-127delinsTG ENSP00000494085.1:n.230-128_230-127delinsTG
ENST00000644810.1:c.230-751_230-750delinsTG ENSP00000495895.1:n.230-751_230-750delinsTG
ENST00000644831.1:n.259-128_259-127delinsTG
ENST00000644933.1:c.-500-128_-500-127delinsTG ENSP00000496133.1:n.-500-128_-500-127delinsTG
ENST00000645020.1:n.1130_1131delinsTG
ENST00000645285.1:c.-500-128_-500-127delinsTG ENSP00000495058.1:n.-500-128_-500-127delinsTG
ENST00000645331.1:n.252-128_252-127delinsTG
ENST00000645620.1:c.-442-128_-442-127delinsTG ENSP00000493657.1:n.-442-128_-442-127delinsTG
ENST00000646777.1:n.259-128_259-127delinsTG
ENST00000647016.1:n.435_436delinsTG
ENST00000647152.1:c.-500-128_-500-127delinsTG ENSP00000495893.1:n.-500-128_-500-127delinsTG
ENST00000647209.1:c.*99-128_*99-127delinsTG ENSP00000495558.1:n.*99-128_*99-127delinsTG
ENST00000647346.1:n.1122_1123delinsTG
ENST00000299427.10:c.230-128_230-127delinsTG ENSP00000299427.6:n.230-128_230-127delinsTG
ENST00000428886.6:n.252-128_252-127delinsTG
ENST00000436873.6:c.230-128_230-127delinsTG ENSP00000398136.2:n.230-128_230-127delinsTG
ENST00000528571.5:c.90-128_90-127delinsTG ENSP00000434647.1:n.90-128_90-127delinsTG
ENST00000528917.1:n.531-128_531-127delinsTG
ENST00000530040.1:n.342-128_342-127delinsTG
ENST00000533371.5:c.-500-128_-500-127delinsTG ENSP00000437066.1:n.-500-128_-500-127delinsTG
ENST00000534644.5:n.215-128_215-127delinsTG
ENST00000611494.4:c.230-128_230-127delinsTG ENSP00000484546.1:n.230-128_230-127delinsTG
NM_000391.3:c.230-128_230-127delinsTG NP_000382.3:n.230-128_230-127delinsTG
NM_000391.4:c.230-128_230-127delinsTG MANE Select NP_000382.3:n.230-128_230-127delinsTG