Canonical Allele Identifier: CA2790314344

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617205_6617206del , CM000673.2:g.6617205_6617206del	GRCh38
NC_000011.9:g.6638436_6638437del , CM000673.1:g.6638436_6638437del	GRCh37
NC_000011.8:g.6595012_6595013del	NCBI36
NG_008653.1:g.7256_7257del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.395-53_395-52del	ENSP00000507321.1:n.395-53_395-52del
ENST00000299427.12:c.509-53_509-52del MANE Select	ENSP00000299427.6:n.509-53_509-52del
ENST00000428886.7:n.691_692del
ENST00000436873.7:c.312+95_312+96del
ENST00000524788.2:n.1615_1616del
ENST00000524903.2:n.1731_1732del
ENST00000528807.2:n.165-53_165-52del
ENST00000530040.2:n.479+153_479+154del
ENST00000533371.6:c.-221-53_-221-52del	ENSP00000437066.1:n.-221-53_-221-52del
ENST00000534644.6:n.457-53_457-52del
ENST00000642892.1:c.-221-53_-221-52del	ENSP00000494165.1:n.-221-53_-221-52del
ENST00000643439.1:c.*249-53_*249-52del	ENSP00000495849.1:n.*249-53_*249-52del
ENST00000643479.1:n.538-53_538-52del
ENST00000643516.1:c.395+95_395+96del
ENST00000644151.1:n.1895_1896del
ENST00000644218.1:c.509-53_509-52del	ENSP00000493574.1:n.509-53_509-52del
ENST00000644683.1:c.451-53_451-52del	ENSP00000494085.1:n.451-53_451-52del
ENST00000644810.1:c.230-53_230-52del	ENSP00000495895.1:n.230-53_230-52del
ENST00000644831.1:n.632_633del
ENST00000644933.1:c.-221-53_-221-52del	ENSP00000496133.1:n.-221-53_-221-52del
ENST00000645020.1:n.1631_1632del
ENST00000645285.1:c.-221-53_-221-52del	ENSP00000495058.1:n.-221-53_-221-52del
ENST00000645331.1:n.822_823del
ENST00000645620.1:c.-221-53_-221-52del	ENSP00000493657.1:n.-221-53_-221-52del
ENST00000646777.1:n.632_633del
ENST00000647016.1:n.936_937del
ENST00000647152.1:c.-221-53_-221-52del	ENSP00000495893.1:n.-221-53_-221-52del
ENST00000647209.1:c.*378-53_*378-52del	ENSP00000495558.1:n.*378-53_*378-52del
ENST00000647346.1:n.1529-53_1529-52del
ENST00000299427.10:c.509-53_509-52del	ENSP00000299427.6:n.509-53_509-52del
ENST00000428886.6:n.625_626del
ENST00000436873.6:c.450+153_450+154del	ENSP00000398136.2:n.450+153_450+154del
ENST00000524788.1:n.156_157del
ENST00000528571.5:c.*249-53_*249-52del	ENSP00000434647.1:n.*249-53_*249-52del
ENST00000528807.1:n.6_7del
ENST00000533371.5:c.-221-53_-221-52del	ENSP00000437066.1:n.-221-53_-221-52del
ENST00000534644.5:n.494-53_494-52del
ENST00000611494.4:c.509-53_509-52del	ENSP00000484546.1:n.509-53_509-52del
NM_000391.3:c.509-53_509-52del	NP_000382.3:n.509-53_509-52del
NM_000391.4:c.509-53_509-52del MANE Select	NP_000382.3:n.509-53_509-52del