Canonical Allele Identifier: CA2790314481

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617999_6618000insACA , CM000673.2:g.6617999_6618000insACA	GRCh38
NC_000011.9:g.6639230_6639231insACA , CM000673.1:g.6639230_6639231insACA	GRCh37
NC_000011.8:g.6595806_6595807insACA	NCBI36
NG_008653.1:g.6462_6463insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.116-224_116-223insTGT	ENSP00000507321.1:n.116-224_116-223insTGT
ENST00000299427.12:c.230-224_230-223insTGT MANE Select	ENSP00000299427.6:n.230-224_230-223insTGT
ENST00000428886.7:n.318-224_318-223insTGT
ENST00000436873.7:c.34-224_34-223insTGT
ENST00000524788.2:n.1018_1019insTGT
ENST00000524903.2:n.1134_1135insTGT
ENST00000528571.6:c.90-224_90-223insTGT	ENSP00000434647.1:n.90-224_90-223insTGT
ENST00000530040.2:n.259-224_259-223insTGT
ENST00000533371.6:c.-500-224_-500-223insTGT	ENSP00000437066.1:n.-500-224_-500-223insTGT
ENST00000534644.6:n.231-224_231-223insTGT
ENST00000642892.1:c.-447-224_-447-223insTGT	ENSP00000494165.1:n.-447-224_-447-223insTGT
ENST00000643439.1:c.90-224_90-223insTGT	ENSP00000495849.1:n.90-224_90-223insTGT
ENST00000643479.1:n.259-224_259-223insTGT
ENST00000643516.1:c.117-224_117-223insTGT
ENST00000644151.1:n.1298_1299insTGT
ENST00000644218.1:c.230-224_230-223insTGT	ENSP00000493574.1:n.230-224_230-223insTGT
ENST00000644683.1:c.230-224_230-223insTGT	ENSP00000494085.1:n.230-224_230-223insTGT
ENST00000644810.1:c.229+776_229+777insTGT	ENSP00000495895.1:n.229+776_229+777insTGT
ENST00000644831.1:n.259-224_259-223insTGT
ENST00000644933.1:c.-500-224_-500-223insTGT	ENSP00000496133.1:n.-500-224_-500-223insTGT
ENST00000645020.1:n.1034_1035insTGT
ENST00000645285.1:c.-500-224_-500-223insTGT	ENSP00000495058.1:n.-500-224_-500-223insTGT
ENST00000645331.1:n.252-224_252-223insTGT
ENST00000645620.1:c.-442-224_-442-223insTGT	ENSP00000493657.1:n.-442-224_-442-223insTGT
ENST00000646777.1:n.259-224_259-223insTGT
ENST00000647016.1:n.339_340insTGT
ENST00000647152.1:c.-500-224_-500-223insTGT	ENSP00000495893.1:n.-500-224_-500-223insTGT
ENST00000647209.1:c.*99-224_*99-223insTGT	ENSP00000495558.1:n.*99-224_*99-223insTGT
ENST00000647346.1:n.1026_1027insTGT
ENST00000299427.10:c.230-224_230-223insTGT	ENSP00000299427.6:n.230-224_230-223insTGT
ENST00000428886.6:n.252-224_252-223insTGT
ENST00000436873.6:c.230-224_230-223insTGT	ENSP00000398136.2:n.230-224_230-223insTGT
ENST00000528571.5:c.90-224_90-223insTGT	ENSP00000434647.1:n.90-224_90-223insTGT
ENST00000528917.1:n.531-224_531-223insTGT
ENST00000530040.1:n.342-224_342-223insTGT
ENST00000533371.5:c.-500-224_-500-223insTGT	ENSP00000437066.1:n.-500-224_-500-223insTGT
ENST00000534644.5:n.215-224_215-223insTGT
ENST00000611494.4:c.230-224_230-223insTGT	ENSP00000484546.1:n.230-224_230-223insTGT
NM_000391.3:c.230-224_230-223insTGT	NP_000382.3:n.230-224_230-223insTGT
NM_000391.4:c.230-224_230-223insTGT MANE Select	NP_000382.3:n.230-224_230-223insTGT