Canonical Allele Identifier: CA1950232735

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614640C= , CM000673.2:g.6614640C=	GRCh38
NC_000011.9:g.6635871C= , CM000673.1:g.6635871C=	GRCh37
NC_000011.8:g.6592447C=	NCBI36
NG_008653.1:g.9822G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1484G=	ENSP00000507321.1:p.Gly495=
ENST00000299427.12:c.1598G= MANE Select	ENSP00000299427.6:p.Gly533=
ENST00000524611.2:n.637G=
ENST00000524924.2:n.718G=
ENST00000533371.6:c.869G=	ENSP00000437066.1:p.Gly290=
ENST00000642892.1:c.869G=	ENSP00000494165.1:p.Gly290=
ENST00000643342.1:c.671G=
ENST00000643439.1:c.*1338G=	ENSP00000495849.1:n.*1338G=
ENST00000643479.1:n.1784G=
ENST00000643516.1:c.1107G=
ENST00000644218.1:c.1409G=	ENSP00000493574.1:p.Gly470=
ENST00000644683.1:c.*1051G=	ENSP00000494085.1:n.*1051G=
ENST00000644810.1:c.1319G=	ENSP00000495895.1:p.Gly440=
ENST00000644831.1:n.1774G=
ENST00000644933.1:c.*464G=	ENSP00000496133.1:n.*464G=
ENST00000645285.1:c.*464G=	ENSP00000495058.1:n.*464G=
ENST00000645331.1:n.2803G=
ENST00000645620.1:c.869G=	ENSP00000493657.1:p.Gly290=
ENST00000646691.1:n.1485G=
ENST00000646777.1:n.1931G=
ENST00000647016.1:n.2078G=
ENST00000647152.1:c.869G=	ENSP00000495893.1:p.Gly290=
ENST00000647209.1:c.*1467G=	ENSP00000495558.1:n.*1467G=
ENST00000647346.1:n.2618G=
ENST00000299427.10:c.1598G=	ENSP00000299427.6:p.Gly533=
ENST00000533371.5:c.869G=	ENSP00000437066.1:p.Gly290=
ENST00000611494.4:c.1598G=	ENSP00000484546.1:p.Gly533=
NM_000391.3:c.1598G=	NP_000382.3:p.Gly533=
NM_000391.4:c.1598G= MANE Select	NP_000382.3:p.Gly533=