Canonical Allele Identifier: CA379472952

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6636719A>C (hg19) ; chr11:g.6615488A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615488A>C , CM000673.2:g.6615488A>C	GRCh38
NC_000011.9:g.6636719A>C , CM000673.1:g.6636719A>C	GRCh37
NC_000011.8:g.6593295A>C	NCBI36
NG_008653.1:g.8974T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1106T>G	ENSP00000507321.1:p.Ile369Ser
ENST00000299427.12:c.1220T>G MANE Select	ENSP00000299427.6:p.Ile407Ser
ENST00000436873.7:c.457T>G
ENST00000524924.2:n.340T>G
ENST00000533371.6:c.491T>G	ENSP00000437066.1:p.Ile164Ser
ENST00000642892.1:c.491T>G	ENSP00000494165.1:p.Ile164Ser
ENST00000643342.1:c.293T>G
ENST00000643439.1:c.*960T>G	ENSP00000495849.1:n.*960T>G
ENST00000643479.1:n.1406T>G
ENST00000643516.1:c.729T>G
ENST00000644218.1:c.1031T>G	ENSP00000493574.1:p.Ile344Ser
ENST00000644683.1:c.*673T>G	ENSP00000494085.1:n.*673T>G
ENST00000644810.1:c.941T>G	ENSP00000495895.1:p.Ile314Ser
ENST00000644831.1:n.1396T>G
ENST00000644933.1:c.*86T>G	ENSP00000496133.1:n.*86T>G
ENST00000645285.1:c.*86T>G	ENSP00000495058.1:n.*86T>G
ENST00000645331.1:n.2425T>G
ENST00000645620.1:c.491T>G	ENSP00000493657.1:p.Ile164Ser
ENST00000646691.1:n.995T>G
ENST00000646777.1:n.1553T>G
ENST00000647016.1:n.1700T>G
ENST00000647152.1:c.491T>G	ENSP00000495893.1:p.Ile164Ser
ENST00000647209.1:c.*1089T>G	ENSP00000495558.1:n.*1089T>G
ENST00000647346.1:n.2240T>G
ENST00000299427.10:c.1220T>G	ENSP00000299427.6:p.Ile407Ser
ENST00000524924.1:n.175T>G
ENST00000532191.1:n.273T>G
ENST00000533371.5:c.491T>G	ENSP00000437066.1:p.Ile164Ser
ENST00000611494.4:c.1220T>G	ENSP00000484546.1:p.Ile407Ser
NM_000391.3:c.1220T>G	NP_000382.3:p.Ile407Ser
NM_000391.4:c.1220T>G MANE Select	NP_000382.3:p.Ile407Ser