Canonical Allele Identifier: CA2790314349

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617222_6617224del , CM000673.2:g.6617222_6617224del	GRCh38
NC_000011.9:g.6638453_6638455del , CM000673.1:g.6638453_6638455del	GRCh37
NC_000011.8:g.6595029_6595031del	NCBI36
NG_008653.1:g.7240_7242del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.395-69_395-67del	ENSP00000507321.1:n.395-69_395-67del
ENST00000299427.12:c.509-69_509-67del MANE Select	ENSP00000299427.6:n.509-69_509-67del
ENST00000428886.7:n.675_677del
ENST00000436873.7:c.312+79_312+81del
ENST00000524788.2:n.1599_1601del
ENST00000524903.2:n.1715_1717del
ENST00000528571.6:c.*327_*329del	ENSP00000434647.1:n.*327_*329del
ENST00000528807.2:n.165-69_165-67del
ENST00000530040.2:n.479+137_479+139del
ENST00000533371.6:c.-221-69_-221-67del	ENSP00000437066.1:n.-221-69_-221-67del
ENST00000534644.6:n.457-69_457-67del
ENST00000642892.1:c.-221-69_-221-67del	ENSP00000494165.1:n.-221-69_-221-67del
ENST00000643439.1:c.*249-69_*249-67del	ENSP00000495849.1:n.*249-69_*249-67del
ENST00000643479.1:n.538-69_538-67del
ENST00000643516.1:c.395+79_395+81del
ENST00000644151.1:n.1879_1881del
ENST00000644218.1:c.509-69_509-67del	ENSP00000493574.1:n.509-69_509-67del
ENST00000644683.1:c.451-69_451-67del	ENSP00000494085.1:n.451-69_451-67del
ENST00000644810.1:c.230-69_230-67del	ENSP00000495895.1:n.230-69_230-67del
ENST00000644831.1:n.616_618del
ENST00000644933.1:c.-221-69_-221-67del	ENSP00000496133.1:n.-221-69_-221-67del
ENST00000645020.1:n.1615_1617del
ENST00000645285.1:c.-221-69_-221-67del	ENSP00000495058.1:n.-221-69_-221-67del
ENST00000645331.1:n.806_808del
ENST00000645620.1:c.-221-69_-221-67del	ENSP00000493657.1:n.-221-69_-221-67del
ENST00000646777.1:n.616_618del
ENST00000647016.1:n.920_922del
ENST00000647152.1:c.-221-69_-221-67del	ENSP00000495893.1:n.-221-69_-221-67del
ENST00000647209.1:c.*378-69_*378-67del	ENSP00000495558.1:n.*378-69_*378-67del
ENST00000647346.1:n.1529-69_1529-67del
ENST00000299427.10:c.509-69_509-67del	ENSP00000299427.6:n.509-69_509-67del
ENST00000428886.6:n.609_611del
ENST00000436873.6:c.450+137_450+139del	ENSP00000398136.2:n.450+137_450+139del
ENST00000524788.1:n.140_142del
ENST00000528571.5:c.*249-69_*249-67del	ENSP00000434647.1:n.*249-69_*249-67del
ENST00000533371.5:c.-221-69_-221-67del	ENSP00000437066.1:n.-221-69_-221-67del
ENST00000534644.5:n.494-69_494-67del
ENST00000611494.4:c.509-69_509-67del	ENSP00000484546.1:n.509-69_509-67del
NM_000391.3:c.509-69_509-67del	NP_000382.3:n.509-69_509-67del
NM_000391.4:c.509-69_509-67del MANE Select	NP_000382.3:n.509-69_509-67del