Canonical Allele Identifier: CA1950232806

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614680G= , CM000673.2:g.6614680G=	GRCh38
NC_000011.9:g.6635911G= , CM000673.1:g.6635911G=	GRCh37
NC_000011.8:g.6592487G=	NCBI36
NG_008653.1:g.9782C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1444C=	ENSP00000507321.1:p.Arg482=
ENST00000299427.12:c.1558C= MANE Select	ENSP00000299427.6:p.Arg520=
ENST00000524611.2:n.597C=
ENST00000524924.2:n.678C=
ENST00000533371.6:c.829C=	ENSP00000437066.1:p.Arg277=
ENST00000642892.1:c.829C=	ENSP00000494165.1:p.Arg277=
ENST00000643342.1:c.631C=
ENST00000643439.1:c.*1298C=	ENSP00000495849.1:n.*1298C=
ENST00000643479.1:n.1744C=
ENST00000643516.1:c.1067C=
ENST00000644218.1:c.1369C=	ENSP00000493574.1:p.Arg457=
ENST00000644683.1:c.*1011C=	ENSP00000494085.1:n.*1011C=
ENST00000644810.1:c.1279C=	ENSP00000495895.1:p.Arg427=
ENST00000644831.1:n.1734C=
ENST00000644933.1:c.*424C=	ENSP00000496133.1:n.*424C=
ENST00000645285.1:c.*424C=	ENSP00000495058.1:n.*424C=
ENST00000645331.1:n.2763C=
ENST00000645620.1:c.829C=	ENSP00000493657.1:p.Arg277=
ENST00000646691.1:n.1445C=
ENST00000646777.1:n.1891C=
ENST00000647016.1:n.2038C=
ENST00000647152.1:c.829C=	ENSP00000495893.1:p.Arg277=
ENST00000647209.1:c.*1427C=	ENSP00000495558.1:n.*1427C=
ENST00000647346.1:n.2578C=
ENST00000299427.10:c.1558C=	ENSP00000299427.6:p.Arg520=
ENST00000524611.1:n.436C=
ENST00000533371.5:c.829C=	ENSP00000437066.1:p.Arg277=
ENST00000611494.4:c.1558C=	ENSP00000484546.1:p.Arg520=
NM_000391.3:c.1558C=	NP_000382.3:p.Arg520=
NM_000391.4:c.1558C= MANE Select	NP_000382.3:p.Arg520=