Canonical Allele Identifier: CA472768832

Gene: TPP1

Linked Data

• gnomAD v4: 11-6614492-C-CT
• MyVariant Identifiers: chr11:g.6635723_6635724insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614493dup , CM000673.2:g.6614493dup	GRCh38
NC_000011.9:g.6635724dup , CM000673.1:g.6635724dup	GRCh37
NC_000011.8:g.6592300dup	NCBI36
NG_008653.1:g.9969dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*53dup	ENSP00000507321.1:n.*53dup
ENST00000299427.12:c.*53dup MANE Select	ENSP00000299427.6:n.*53dup
ENST00000524611.2:n.784dup
ENST00000533371.6:c.*53dup	ENSP00000437066.1:n.*53dup
ENST00000642892.1:c.*53dup	ENSP00000494165.1:n.*53dup
ENST00000643342.1:c.818dup
ENST00000643439.1:c.*1485dup	ENSP00000495849.1:n.*1485dup
ENST00000643479.1:n.1931dup
ENST00000643516.1:c.1254dup
ENST00000644218.1:c.*53dup	ENSP00000493574.1:n.*53dup
ENST00000644683.1:c.*1198dup	ENSP00000494085.1:n.*1198dup
ENST00000644810.1:c.*53dup	ENSP00000495895.1:n.*53dup
ENST00000644831.1:n.1921dup
ENST00000644933.1:c.*611dup	ENSP00000496133.1:n.*611dup
ENST00000645285.1:c.*611dup	ENSP00000495058.1:n.*611dup
ENST00000645331.1:n.2950dup
ENST00000645620.1:c.*53dup	ENSP00000493657.1:n.*53dup
ENST00000646691.1:n.1632dup
ENST00000646777.1:n.2078dup
ENST00000647016.1:n.2225dup
ENST00000647152.1:c.*53dup	ENSP00000495893.1:n.*53dup
ENST00000647209.1:c.*1614dup	ENSP00000495558.1:n.*1614dup
ENST00000647346.1:n.2765dup
ENST00000299427.10:c.*53dup	ENSP00000299427.6:n.*53dup
ENST00000533371.5:c.*53dup	ENSP00000437066.1:n.*53dup
ENST00000611494.4:c.*73dup	ENSP00000484546.1:n.*73dup
NM_000391.3:c.*53dup	NP_000382.3:n.*53dup
NM_000391.4:c.*53dup MANE Select	NP_000382.3:n.*53dup