Canonical Allele Identifier: CA2790314337

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617181_6617182insG , CM000673.2:g.6617181_6617182insG	GRCh38
NC_000011.9:g.6638412_6638413insG , CM000673.1:g.6638412_6638413insG	GRCh37
NC_000011.8:g.6594988_6594989insG	NCBI36
NG_008653.1:g.7280_7281insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.395-29_395-28insC	ENSP00000507321.1:n.395-29_395-28insC
ENST00000299427.12:c.509-29_509-28insC MANE Select	ENSP00000299427.6:n.509-29_509-28insC
ENST00000428886.7:n.715_716insC
ENST00000436873.7:c.312+119_312+120insC
ENST00000524788.2:n.1639_1640insC
ENST00000524903.2:n.1755_1756insC
ENST00000528807.2:n.165-29_165-28insC
ENST00000530040.2:n.479+177_479+178insC
ENST00000533371.6:c.-221-29_-221-28insC	ENSP00000437066.1:n.-221-29_-221-28insC
ENST00000534644.6:n.457-29_457-28insC
ENST00000642892.1:c.-221-29_-221-28insC	ENSP00000494165.1:n.-221-29_-221-28insC
ENST00000643439.1:c.*249-29_*249-28insC	ENSP00000495849.1:n.*249-29_*249-28insC
ENST00000643479.1:n.538-29_538-28insC
ENST00000643516.1:c.395+119_395+120insC
ENST00000644151.1:n.1919_1920insC
ENST00000644218.1:c.509-29_509-28insC	ENSP00000493574.1:n.509-29_509-28insC
ENST00000644683.1:c.451-29_451-28insC	ENSP00000494085.1:n.451-29_451-28insC
ENST00000644810.1:c.230-29_230-28insC	ENSP00000495895.1:n.230-29_230-28insC
ENST00000644831.1:n.656_657insC
ENST00000644933.1:c.-221-29_-221-28insC	ENSP00000496133.1:n.-221-29_-221-28insC
ENST00000645020.1:n.1655_1656insC
ENST00000645285.1:c.-221-29_-221-28insC	ENSP00000495058.1:n.-221-29_-221-28insC
ENST00000645331.1:n.846_847insC
ENST00000645620.1:c.-221-29_-221-28insC	ENSP00000493657.1:n.-221-29_-221-28insC
ENST00000646777.1:n.656_657insC
ENST00000647016.1:n.960_961insC
ENST00000647152.1:c.-221-29_-221-28insC	ENSP00000495893.1:n.-221-29_-221-28insC
ENST00000647209.1:c.*378-29_*378-28insC	ENSP00000495558.1:n.*378-29_*378-28insC
ENST00000647346.1:n.1529-29_1529-28insC
ENST00000299427.10:c.509-29_509-28insC	ENSP00000299427.6:n.509-29_509-28insC
ENST00000428886.6:n.649_650insC
ENST00000436873.6:c.450+177_450+178insC	ENSP00000398136.2:n.450+177_450+178insC
ENST00000524788.1:n.180_181insC
ENST00000528571.5:c.*249-29_*249-28insC	ENSP00000434647.1:n.*249-29_*249-28insC
ENST00000528807.1:n.30_31insC
ENST00000533371.5:c.-221-29_-221-28insC	ENSP00000437066.1:n.-221-29_-221-28insC
ENST00000534644.5:n.494-29_494-28insC
ENST00000611494.4:c.509-29_509-28insC	ENSP00000484546.1:n.509-29_509-28insC
NM_000391.3:c.509-29_509-28insC	NP_000382.3:n.509-29_509-28insC
NM_000391.4:c.509-29_509-28insC MANE Select	NP_000382.3:n.509-29_509-28insC