Canonical Allele Identifier: CA2790314293

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616537_6616538insAGC , CM000673.2:g.6616537_6616538insAGC	GRCh38
NC_000011.9:g.6637768_6637769insAGC , CM000673.1:g.6637768_6637769insAGC	GRCh37
NC_000011.8:g.6594344_6594345insAGC	NCBI36
NG_008653.1:g.7924_7925insGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.773-35_773-34insGCT	ENSP00000507321.1:n.773-35_773-34insGCT
ENST00000299427.12:c.887-35_887-34insGCT MANE Select	ENSP00000299427.6:n.887-35_887-34insGCT
ENST00000436873.7:c.313-464_313-463insGCT
ENST00000524903.2:n.2284_2285insGCT
ENST00000530040.2:n.480-35_480-34insGCT
ENST00000533371.6:c.158-35_158-34insGCT	ENSP00000437066.1:n.158-35_158-34insGCT
ENST00000642892.1:c.158-35_158-34insGCT	ENSP00000494165.1:n.158-35_158-34insGCT
ENST00000643439.1:c.*627-35_*627-34insGCT	ENSP00000495849.1:n.*627-35_*627-34insGCT
ENST00000643479.1:n.1038_1039insGCT
ENST00000643516.1:c.396-35_396-34insGCT
ENST00000644218.1:c.886+123_886+124insGCT	ENSP00000493574.1:n.886+123_886+124insGCT
ENST00000644683.1:c.*340-35_*340-34insGCT	ENSP00000494085.1:n.*340-35_*340-34insGCT
ENST00000644810.1:c.608-35_608-34insGCT	ENSP00000495895.1:n.608-35_608-34insGCT
ENST00000644831.1:n.1063-35_1063-34insGCT
ENST00000644933.1:c.158-35_158-34insGCT	ENSP00000496133.1:n.158-35_158-34insGCT
ENST00000645285.1:c.157+123_157+124insGCT	ENSP00000495058.1:n.157+123_157+124insGCT
ENST00000645331.1:n.1375_1376insGCT
ENST00000645620.1:c.158-35_158-34insGCT	ENSP00000493657.1:n.158-35_158-34insGCT
ENST00000646777.1:n.1185_1186insGCT
ENST00000647016.1:n.1367-35_1367-34insGCT
ENST00000647152.1:c.158-35_158-34insGCT	ENSP00000495893.1:n.158-35_158-34insGCT
ENST00000647209.1:c.*756-35_*756-34insGCT	ENSP00000495558.1:n.*756-35_*756-34insGCT
ENST00000647346.1:n.1907-35_1907-34insGCT
ENST00000299427.10:c.887-35_887-34insGCT	ENSP00000299427.6:n.887-35_887-34insGCT
ENST00000436873.6:c.451-35_451-34insGCT	ENSP00000398136.2:n.451-35_451-34insGCT
ENST00000528807.1:n.559_560insGCT
ENST00000533371.5:c.158-35_158-34insGCT	ENSP00000437066.1:n.158-35_158-34insGCT
ENST00000611494.4:c.887-35_887-34insGCT	ENSP00000484546.1:n.887-35_887-34insGCT
NM_000391.3:c.887-35_887-34insGCT	NP_000382.3:n.887-35_887-34insGCT
NM_000391.4:c.887-35_887-34insGCT MANE Select	NP_000382.3:n.887-35_887-34insGCT