Canonical Allele Identifier: CA379473042

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6636749A>T (hg19) ; chr11:g.6615518A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615518A>T , CM000673.2:g.6615518A>T	GRCh38
NC_000011.9:g.6636749A>T , CM000673.1:g.6636749A>T	GRCh37
NC_000011.8:g.6593325A>T	NCBI36
NG_008653.1:g.8944T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1076T>A	ENSP00000507321.1:p.Phe359Tyr
ENST00000299427.12:c.1190T>A MANE Select	ENSP00000299427.6:p.Phe397Tyr
ENST00000436873.7:c.427T>A
ENST00000524924.2:n.310T>A
ENST00000533371.6:c.461T>A	ENSP00000437066.1:p.Phe154Tyr
ENST00000642892.1:c.461T>A	ENSP00000494165.1:p.Phe154Tyr
ENST00000643342.1:c.263T>A
ENST00000643439.1:c.*930T>A	ENSP00000495849.1:n.*930T>A
ENST00000643479.1:n.1376T>A
ENST00000643516.1:c.699T>A
ENST00000644218.1:c.1001T>A	ENSP00000493574.1:p.Phe334Tyr
ENST00000644683.1:c.*643T>A	ENSP00000494085.1:n.*643T>A
ENST00000644810.1:c.911T>A	ENSP00000495895.1:p.Phe304Tyr
ENST00000644831.1:n.1366T>A
ENST00000644933.1:c.*56T>A	ENSP00000496133.1:n.*56T>A
ENST00000645285.1:c.*56T>A	ENSP00000495058.1:n.*56T>A
ENST00000645331.1:n.2395T>A
ENST00000645620.1:c.461T>A	ENSP00000493657.1:p.Phe154Tyr
ENST00000646691.1:n.965T>A
ENST00000646777.1:n.1523T>A
ENST00000647016.1:n.1670T>A
ENST00000647152.1:c.461T>A	ENSP00000495893.1:p.Phe154Tyr
ENST00000647209.1:c.*1059T>A	ENSP00000495558.1:n.*1059T>A
ENST00000647346.1:n.2210T>A
ENST00000299427.10:c.1190T>A	ENSP00000299427.6:p.Phe397Tyr
ENST00000524924.1:n.145T>A
ENST00000532191.1:n.243T>A
ENST00000533371.5:c.461T>A	ENSP00000437066.1:p.Phe154Tyr
ENST00000611494.4:c.1190T>A	ENSP00000484546.1:p.Phe397Tyr
NM_000391.3:c.1190T>A	NP_000382.3:p.Phe397Tyr
NM_000391.4:c.1190T>A MANE Select	NP_000382.3:p.Phe397Tyr