Canonical Allele Identifier: CA379472890

Gene: TPP1

Linked Data

• COSMIC: COSM1492693
• MyVariant Identifiers: chr11:g.6636691G>T (hg19) ; chr11:g.6615460G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615460G>T , CM000673.2:g.6615460G>T	GRCh38
NC_000011.9:g.6636691G>T , CM000673.1:g.6636691G>T	GRCh37
NC_000011.8:g.6593267G>T	NCBI36
NG_008653.1:g.9002C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1134C>A	ENSP00000507321.1:p.Phe378Leu
ENST00000299427.12:c.1248C>A MANE Select	ENSP00000299427.6:p.Phe416Leu
ENST00000436873.7:c.485C>A
ENST00000524924.2:n.368C>A
ENST00000533371.6:c.519C>A	ENSP00000437066.1:p.Phe173Leu
ENST00000642892.1:c.519C>A	ENSP00000494165.1:p.Phe173Leu
ENST00000643342.1:c.321C>A
ENST00000643439.1:c.*988C>A	ENSP00000495849.1:n.*988C>A
ENST00000643479.1:n.1434C>A
ENST00000643516.1:c.757C>A
ENST00000644218.1:c.1059C>A	ENSP00000493574.1:p.Phe353Leu
ENST00000644683.1:c.*701C>A	ENSP00000494085.1:n.*701C>A
ENST00000644810.1:c.969C>A	ENSP00000495895.1:p.Phe323Leu
ENST00000644831.1:n.1424C>A
ENST00000644933.1:c.*114C>A	ENSP00000496133.1:n.*114C>A
ENST00000645285.1:c.*114C>A	ENSP00000495058.1:n.*114C>A
ENST00000645331.1:n.2453C>A
ENST00000645620.1:c.519C>A	ENSP00000493657.1:p.Phe173Leu
ENST00000646691.1:n.1023C>A
ENST00000646777.1:n.1581C>A
ENST00000647016.1:n.1728C>A
ENST00000647152.1:c.519C>A	ENSP00000495893.1:p.Phe173Leu
ENST00000647209.1:c.*1117C>A	ENSP00000495558.1:n.*1117C>A
ENST00000647346.1:n.2268C>A
ENST00000299427.10:c.1248C>A	ENSP00000299427.6:p.Phe416Leu
ENST00000524611.1:n.14C>A
ENST00000524924.1:n.203C>A
ENST00000532191.1:n.301C>A
ENST00000533371.5:c.519C>A	ENSP00000437066.1:p.Phe173Leu
ENST00000611494.4:c.1248C>A	ENSP00000484546.1:p.Phe416Leu
NM_000391.3:c.1248C>A	NP_000382.3:p.Phe416Leu
NM_000391.4:c.1248C>A MANE Select	NP_000382.3:p.Phe416Leu