Canonical Allele Identifier: CA2612256358

Gene: TPP1

Linked Data

• gnomAD v4: 11-6614534-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614535del , CM000673.2:g.6614535del	GRCh38
NC_000011.9:g.6635766del , CM000673.1:g.6635766del	GRCh37
NC_000011.8:g.6592342del	NCBI36
NG_008653.1:g.9927del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*11del	ENSP00000507321.1:n.*11del
ENST00000299427.12:c.*11del MANE Select	ENSP00000299427.6:n.*11del
ENST00000524611.2:n.742del
ENST00000533371.6:c.*11del	ENSP00000437066.1:n.*11del
ENST00000642892.1:c.*11del	ENSP00000494165.1:n.*11del
ENST00000643342.1:c.776del
ENST00000643439.1:c.*1443del	ENSP00000495849.1:n.*1443del
ENST00000643479.1:n.1889del
ENST00000643516.1:c.1212del
ENST00000644218.1:c.*11del	ENSP00000493574.1:n.*11del
ENST00000644683.1:c.*1156del	ENSP00000494085.1:n.*1156del
ENST00000644810.1:c.*11del	ENSP00000495895.1:n.*11del
ENST00000644831.1:n.1879del
ENST00000644933.1:c.*569del	ENSP00000496133.1:n.*569del
ENST00000645285.1:c.*569del	ENSP00000495058.1:n.*569del
ENST00000645331.1:n.2908del
ENST00000645620.1:c.*11del	ENSP00000493657.1:n.*11del
ENST00000646691.1:n.1590del
ENST00000646777.1:n.2036del
ENST00000647016.1:n.2183del
ENST00000647152.1:c.*11del	ENSP00000495893.1:n.*11del
ENST00000647209.1:c.*1572del	ENSP00000495558.1:n.*1572del
ENST00000647346.1:n.2723del
ENST00000299427.10:c.*11del	ENSP00000299427.6:n.*11del
ENST00000533371.5:c.*11del	ENSP00000437066.1:n.*11del
ENST00000611494.4:c.*31del	ENSP00000484546.1:n.*31del
NM_000391.3:c.*11del	NP_000382.3:n.*11del
NM_000391.4:c.*11del MANE Select	NP_000382.3:n.*11del