Canonical Allele Identifier: CA379475999

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638630T>A (hg19) ; chr11:g.6617399T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617399T>A , CM000673.2:g.6617399T>A	GRCh38
NC_000011.9:g.6638630T>A , CM000673.1:g.6638630T>A	GRCh37
NC_000011.8:g.6595206T>A	NCBI36
NG_008653.1:g.7063A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.296A>T	ENSP00000507321.1:p.Glu99Val
ENST00000299427.12:c.410A>T MANE Select	ENSP00000299427.6:p.Glu137Val
ENST00000428886.7:n.498A>T
ENST00000436873.7:c.214A>T
ENST00000524788.2:n.1422A>T
ENST00000524903.2:n.1538A>T
ENST00000528571.6:c.*150A>T	ENSP00000434647.1:n.*150A>T
ENST00000528807.2:n.66A>T
ENST00000530040.2:n.439A>T
ENST00000533371.6:c.-320A>T	ENSP00000437066.1:n.-320A>T
ENST00000534644.6:n.411A>T
ENST00000642892.1:c.-267A>T	ENSP00000494165.1:n.-267A>T
ENST00000643439.1:c.*150A>T	ENSP00000495849.1:n.*150A>T
ENST00000643479.1:n.439A>T
ENST00000643516.1:c.297A>T
ENST00000644151.1:n.1702A>T
ENST00000644218.1:c.410A>T	ENSP00000493574.1:p.Glu137Val
ENST00000644683.1:c.410A>T	ENSP00000494085.1:p.Glu137Val
ENST00000644810.1:c.230-246A>T	ENSP00000495895.1:n.230-246A>T
ENST00000644831.1:n.439A>T
ENST00000644933.1:c.-320A>T	ENSP00000496133.1:n.-320A>T
ENST00000645020.1:n.1438A>T
ENST00000645285.1:c.-320A>T	ENSP00000495058.1:n.-320A>T
ENST00000645331.1:n.629A>T
ENST00000645620.1:c.-262A>T	ENSP00000493657.1:n.-262A>T
ENST00000646777.1:n.439A>T
ENST00000647016.1:n.743A>T
ENST00000647152.1:c.-320A>T	ENSP00000495893.1:n.-320A>T
ENST00000647209.1:c.*279A>T	ENSP00000495558.1:n.*279A>T
ENST00000647346.1:n.1430A>T
ENST00000299427.10:c.410A>T	ENSP00000299427.6:p.Glu137Val
ENST00000428886.6:n.432A>T
ENST00000436873.6:c.410A>T	ENSP00000398136.2:p.Glu137Val
ENST00000528571.5:c.*150A>T	ENSP00000434647.1:n.*150A>T
ENST00000530040.1:n.522A>T
ENST00000533371.5:c.-320A>T	ENSP00000437066.1:n.-320A>T
ENST00000534644.5:n.395A>T
ENST00000611494.4:c.410A>T	ENSP00000484546.1:p.Glu137Val
NM_000391.3:c.410A>T	NP_000382.3:p.Glu137Val
NM_000391.4:c.410A>T MANE Select	NP_000382.3:p.Glu137Val