Canonical Allele Identifier: CA2790314473

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617980_6617981insAG , CM000673.2:g.6617980_6617981insAG	GRCh38
NC_000011.9:g.6639211_6639212insAG , CM000673.1:g.6639211_6639212insAG	GRCh37
NC_000011.8:g.6595787_6595788insAG	NCBI36
NG_008653.1:g.6481_6482insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.116-205_116-204insCT	ENSP00000507321.1:n.116-205_116-204insCT
ENST00000299427.12:c.230-205_230-204insCT MANE Select	ENSP00000299427.6:n.230-205_230-204insCT
ENST00000428886.7:n.318-205_318-204insCT
ENST00000436873.7:c.34-205_34-204insCT
ENST00000524788.2:n.1037_1038insCT
ENST00000524903.2:n.1153_1154insCT
ENST00000528571.6:c.90-205_90-204insCT	ENSP00000434647.1:n.90-205_90-204insCT
ENST00000530040.2:n.259-205_259-204insCT
ENST00000533371.6:c.-500-205_-500-204insCT	ENSP00000437066.1:n.-500-205_-500-204insCT
ENST00000534644.6:n.231-205_231-204insCT
ENST00000642892.1:c.-447-205_-447-204insCT	ENSP00000494165.1:n.-447-205_-447-204insCT
ENST00000643439.1:c.90-205_90-204insCT	ENSP00000495849.1:n.90-205_90-204insCT
ENST00000643479.1:n.259-205_259-204insCT
ENST00000643516.1:c.117-205_117-204insCT
ENST00000644151.1:n.1317_1318insCT
ENST00000644218.1:c.230-205_230-204insCT	ENSP00000493574.1:n.230-205_230-204insCT
ENST00000644683.1:c.230-205_230-204insCT	ENSP00000494085.1:n.230-205_230-204insCT
ENST00000644810.1:c.229+795_229+796insCT	ENSP00000495895.1:n.229+795_229+796insCT
ENST00000644831.1:n.259-205_259-204insCT
ENST00000644933.1:c.-500-205_-500-204insCT	ENSP00000496133.1:n.-500-205_-500-204insCT
ENST00000645020.1:n.1053_1054insCT
ENST00000645285.1:c.-500-205_-500-204insCT	ENSP00000495058.1:n.-500-205_-500-204insCT
ENST00000645331.1:n.252-205_252-204insCT
ENST00000645620.1:c.-442-205_-442-204insCT	ENSP00000493657.1:n.-442-205_-442-204insCT
ENST00000646777.1:n.259-205_259-204insCT
ENST00000647016.1:n.358_359insCT
ENST00000647152.1:c.-500-205_-500-204insCT	ENSP00000495893.1:n.-500-205_-500-204insCT
ENST00000647209.1:c.*99-205_*99-204insCT	ENSP00000495558.1:n.*99-205_*99-204insCT
ENST00000647346.1:n.1045_1046insCT
ENST00000299427.10:c.230-205_230-204insCT	ENSP00000299427.6:n.230-205_230-204insCT
ENST00000428886.6:n.252-205_252-204insCT
ENST00000436873.6:c.230-205_230-204insCT	ENSP00000398136.2:n.230-205_230-204insCT
ENST00000528571.5:c.90-205_90-204insCT	ENSP00000434647.1:n.90-205_90-204insCT
ENST00000528917.1:n.531-205_531-204insCT
ENST00000530040.1:n.342-205_342-204insCT
ENST00000533371.5:c.-500-205_-500-204insCT	ENSP00000437066.1:n.-500-205_-500-204insCT
ENST00000534644.5:n.215-205_215-204insCT
ENST00000611494.4:c.230-205_230-204insCT	ENSP00000484546.1:n.230-205_230-204insCT
NM_000391.3:c.230-205_230-204insCT	NP_000382.3:n.230-205_230-204insCT
NM_000391.4:c.230-205_230-204insCT MANE Select	NP_000382.3:n.230-205_230-204insCT