Canonical Allele Identifier: CA2790314449

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617943_6617944insACAC , CM000673.2:g.6617943_6617944insACAC	GRCh38
NC_000011.9:g.6639174_6639175insACAC , CM000673.1:g.6639174_6639175insACAC	GRCh37
NC_000011.8:g.6595750_6595751insACAC	NCBI36
NG_008653.1:g.6518_6519insGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.116-168_116-167insGTGT	ENSP00000507321.1:n.116-168_116-167insGTGT
ENST00000299427.12:c.230-168_230-167insGTGT MANE Select	ENSP00000299427.6:n.230-168_230-167insGTGT
ENST00000428886.7:n.318-168_318-167insGTGT
ENST00000436873.7:c.34-168_34-167insGTGT
ENST00000524788.2:n.1074_1075insGTGT
ENST00000524903.2:n.1190_1191insGTGT
ENST00000528571.6:c.90-168_90-167insGTGT	ENSP00000434647.1:n.90-168_90-167insGTGT
ENST00000530040.2:n.259-168_259-167insGTGT
ENST00000533371.6:c.-500-168_-500-167insGTGT	ENSP00000437066.1:n.-500-168_-500-167insGTGT
ENST00000534644.6:n.231-168_231-167insGTGT
ENST00000642892.1:c.-447-168_-447-167insGTGT	ENSP00000494165.1:n.-447-168_-447-167insGTGT
ENST00000643439.1:c.90-168_90-167insGTGT	ENSP00000495849.1:n.90-168_90-167insGTGT
ENST00000643479.1:n.259-168_259-167insGTGT
ENST00000643516.1:c.117-168_117-167insGTGT
ENST00000644151.1:n.1354_1355insGTGT
ENST00000644218.1:c.230-168_230-167insGTGT	ENSP00000493574.1:n.230-168_230-167insGTGT
ENST00000644683.1:c.230-168_230-167insGTGT	ENSP00000494085.1:n.230-168_230-167insGTGT
ENST00000644810.1:c.230-791_230-790insGTGT	ENSP00000495895.1:n.230-791_230-790insGTGT
ENST00000644831.1:n.259-168_259-167insGTGT
ENST00000644933.1:c.-500-168_-500-167insGTGT	ENSP00000496133.1:n.-500-168_-500-167insGTGT
ENST00000645020.1:n.1090_1091insGTGT
ENST00000645285.1:c.-500-168_-500-167insGTGT	ENSP00000495058.1:n.-500-168_-500-167insGTGT
ENST00000645331.1:n.252-168_252-167insGTGT
ENST00000645620.1:c.-442-168_-442-167insGTGT	ENSP00000493657.1:n.-442-168_-442-167insGTGT
ENST00000646777.1:n.259-168_259-167insGTGT
ENST00000647016.1:n.395_396insGTGT
ENST00000647152.1:c.-500-168_-500-167insGTGT	ENSP00000495893.1:n.-500-168_-500-167insGTGT
ENST00000647209.1:c.*99-168_*99-167insGTGT	ENSP00000495558.1:n.*99-168_*99-167insGTGT
ENST00000647346.1:n.1082_1083insGTGT
ENST00000299427.10:c.230-168_230-167insGTGT	ENSP00000299427.6:n.230-168_230-167insGTGT
ENST00000428886.6:n.252-168_252-167insGTGT
ENST00000436873.6:c.230-168_230-167insGTGT	ENSP00000398136.2:n.230-168_230-167insGTGT
ENST00000528571.5:c.90-168_90-167insGTGT	ENSP00000434647.1:n.90-168_90-167insGTGT
ENST00000528917.1:n.531-168_531-167insGTGT
ENST00000530040.1:n.342-168_342-167insGTGT
ENST00000533371.5:c.-500-168_-500-167insGTGT	ENSP00000437066.1:n.-500-168_-500-167insGTGT
ENST00000534644.5:n.215-168_215-167insGTGT
ENST00000611494.4:c.230-168_230-167insGTGT	ENSP00000484546.1:n.230-168_230-167insGTGT
NM_000391.3:c.230-168_230-167insGTGT	NP_000382.3:n.230-168_230-167insGTGT
NM_000391.4:c.230-168_230-167insGTGT MANE Select	NP_000382.3:n.230-168_230-167insGTGT