Canonical Allele Identifier: CA2697548402

Gene: TPP1

Linked Data

• ClinVar Variation Id: 2755505
• ClinVar RCV Id: RCV003564378

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616659del , CM000673.2:g.6616659del	GRCh38
NC_000011.9:g.6637890del , CM000673.1:g.6637890del	GRCh37
NC_000011.8:g.6594466del	NCBI36
NG_008653.1:g.7803del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.772+2del	ENSP00000507321.1:n.772+2del
ENST00000299427.12:c.886+2del MANE Select	ENSP00000299427.6:n.886+2del
ENST00000436873.7:c.313-585del
ENST00000524788.2:n.2047del
ENST00000524903.2:n.2163del
ENST00000528807.2:n.544del
ENST00000530040.2:n.480-156del
ENST00000533371.6:c.157+2del	ENSP00000437066.1:n.157+2del
ENST00000642892.1:c.157+2del	ENSP00000494165.1:n.157+2del
ENST00000643439.1:c.*626+2del	ENSP00000495849.1:n.*626+2del
ENST00000643479.1:n.917del
ENST00000643516.1:c.396-156del
ENST00000644151.1:n.2327del
ENST00000644218.1:c.886+2del	ENSP00000493574.1:n.886+2del
ENST00000644683.1:c.*339+2del	ENSP00000494085.1:n.*339+2del
ENST00000644810.1:c.607+2del	ENSP00000495895.1:n.607+2del
ENST00000644831.1:n.1062+2del
ENST00000644933.1:c.157+2del	ENSP00000496133.1:n.157+2del
ENST00000645020.1:n.2178del
ENST00000645285.1:c.157+2del	ENSP00000495058.1:n.157+2del
ENST00000645331.1:n.1254del
ENST00000645620.1:c.157+2del	ENSP00000493657.1:n.157+2del
ENST00000646777.1:n.1064del
ENST00000647016.1:n.1366+2del
ENST00000647152.1:c.157+2del	ENSP00000495893.1:n.157+2del
ENST00000647209.1:c.*755+2del	ENSP00000495558.1:n.*755+2del
ENST00000647346.1:n.1906+2del
ENST00000299427.10:c.886+2del	ENSP00000299427.6:n.886+2del
ENST00000436873.6:c.451-156del	ENSP00000398136.2:n.451-156del
ENST00000528807.1:n.438del
ENST00000533371.5:c.157+2del	ENSP00000437066.1:n.157+2del
ENST00000611494.4:c.886+2del	ENSP00000484546.1:n.886+2del
NM_000391.3:c.886+2del	NP_000382.3:n.886+2del
NM_000391.4:c.886+2del MANE Select	NP_000382.3:n.886+2del