Canonical Allele Identifier: CA379475802

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638576T>C (hg19) ; chr11:g.6617345T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617345T>C , CM000673.2:g.6617345T>C	GRCh38
NC_000011.9:g.6638576T>C , CM000673.1:g.6638576T>C	GRCh37
NC_000011.8:g.6595152T>C	NCBI36
NG_008653.1:g.7117A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.350A>G	ENSP00000507321.1:p.His117Arg
ENST00000299427.12:c.464A>G MANE Select	ENSP00000299427.6:p.His155Arg
ENST00000428886.7:n.552A>G
ENST00000436873.7:c.268A>G
ENST00000524788.2:n.1476A>G
ENST00000524903.2:n.1592A>G
ENST00000528571.6:c.*204A>G	ENSP00000434647.1:n.*204A>G
ENST00000528807.2:n.120A>G
ENST00000530040.2:n.479+14A>G
ENST00000533371.6:c.-266A>G	ENSP00000437066.1:n.-266A>G
ENST00000534644.6:n.456+9A>G
ENST00000642892.1:c.-222+9A>G	ENSP00000494165.1:n.-222+9A>G
ENST00000643439.1:c.*204A>G	ENSP00000495849.1:n.*204A>G
ENST00000643479.1:n.493A>G
ENST00000643516.1:c.351A>G
ENST00000644151.1:n.1756A>G
ENST00000644218.1:c.464A>G	ENSP00000493574.1:p.His155Arg
ENST00000644683.1:c.450+14A>G	ENSP00000494085.1:n.450+14A>G
ENST00000644810.1:c.230-192A>G	ENSP00000495895.1:n.230-192A>G
ENST00000644831.1:n.493A>G
ENST00000644933.1:c.-266A>G	ENSP00000496133.1:n.-266A>G
ENST00000645020.1:n.1492A>G
ENST00000645285.1:c.-266A>G	ENSP00000495058.1:n.-266A>G
ENST00000645331.1:n.683A>G
ENST00000645620.1:c.-222+14A>G	ENSP00000493657.1:n.-222+14A>G
ENST00000646777.1:n.493A>G
ENST00000647016.1:n.797A>G
ENST00000647152.1:c.-266A>G	ENSP00000495893.1:n.-266A>G
ENST00000647209.1:c.*333A>G	ENSP00000495558.1:n.*333A>G
ENST00000647346.1:n.1484A>G
ENST00000299427.10:c.464A>G	ENSP00000299427.6:p.His155Arg
ENST00000428886.6:n.486A>G
ENST00000436873.6:c.450+14A>G	ENSP00000398136.2:n.450+14A>G
ENST00000524788.1:n.17A>G
ENST00000528571.5:c.*204A>G	ENSP00000434647.1:n.*204A>G
ENST00000533371.5:c.-266A>G	ENSP00000437066.1:n.-266A>G
ENST00000534644.5:n.449A>G
ENST00000611494.4:c.464A>G	ENSP00000484546.1:p.His155Arg
NM_000391.3:c.464A>G	NP_000382.3:p.His155Arg
NM_000391.4:c.464A>G MANE Select	NP_000382.3:p.His155Arg