Canonical Allele Identifier: CA379472058

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6635840A>T (hg19) ; chr11:g.6614609A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614609A>T , CM000673.2:g.6614609A>T	GRCh38
NC_000011.9:g.6635840A>T , CM000673.1:g.6635840A>T	GRCh37
NC_000011.8:g.6592416A>T	NCBI36
NG_008653.1:g.9853T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.1515T>A	ENSP00000507321.1:p.Asp505Glu
ENST00000299427.12:c.1629T>A MANE Select	ENSP00000299427.6:p.Asp543Glu
ENST00000524611.2:n.668T>A
ENST00000524924.2:n.749T>A
ENST00000533371.6:c.900T>A	ENSP00000437066.1:p.Asp300Glu
ENST00000642892.1:c.900T>A	ENSP00000494165.1:p.Asp300Glu
ENST00000643342.1:c.702T>A
ENST00000643439.1:c.*1369T>A	ENSP00000495849.1:n.*1369T>A
ENST00000643479.1:n.1815T>A
ENST00000643516.1:c.1138T>A
ENST00000644218.1:c.1440T>A	ENSP00000493574.1:p.Asp480Glu
ENST00000644683.1:c.*1082T>A	ENSP00000494085.1:n.*1082T>A
ENST00000644810.1:c.1350T>A	ENSP00000495895.1:p.Asp450Glu
ENST00000644831.1:n.1805T>A
ENST00000644933.1:c.*495T>A	ENSP00000496133.1:n.*495T>A
ENST00000645285.1:c.*495T>A	ENSP00000495058.1:n.*495T>A
ENST00000645331.1:n.2834T>A
ENST00000645620.1:c.900T>A	ENSP00000493657.1:p.Asp300Glu
ENST00000646691.1:n.1516T>A
ENST00000646777.1:n.1962T>A
ENST00000647016.1:n.2109T>A
ENST00000647152.1:c.900T>A	ENSP00000495893.1:p.Asp300Glu
ENST00000647209.1:c.*1498T>A	ENSP00000495558.1:n.*1498T>A
ENST00000647346.1:n.2649T>A
ENST00000299427.10:c.1629T>A	ENSP00000299427.6:p.Asp543Glu
ENST00000533371.5:c.900T>A	ENSP00000437066.1:p.Asp300Glu
ENST00000611494.4:c.1629T>A	ENSP00000484546.1:p.Asp543Glu
NM_000391.3:c.1629T>A	NP_000382.3:p.Asp543Glu
NM_000391.4:c.1629T>A MANE Select	NP_000382.3:p.Asp543Glu