Canonical Allele Identifier: CA1950232500

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614517G= , CM000673.2:g.6614517G=	GRCh38
NC_000011.9:g.6635748G= , CM000673.1:g.6635748G=	GRCh37
NC_000011.8:g.6592324G=	NCBI36
NG_008653.1:g.9945C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*29C=	ENSP00000507321.1:n.*29C=
ENST00000299427.12:c.*29C= MANE Select	ENSP00000299427.6:n.*29C=
ENST00000524611.2:n.760C=
ENST00000533371.6:c.*29C=	ENSP00000437066.1:n.*29C=
ENST00000642892.1:c.*29C=	ENSP00000494165.1:n.*29C=
ENST00000643342.1:c.794C=
ENST00000643439.1:c.*1461C=	ENSP00000495849.1:n.*1461C=
ENST00000643479.1:n.1907C=
ENST00000643516.1:c.1230C=
ENST00000644218.1:c.*29C=	ENSP00000493574.1:n.*29C=
ENST00000644683.1:c.*1174C=	ENSP00000494085.1:n.*1174C=
ENST00000644810.1:c.*29C=	ENSP00000495895.1:n.*29C=
ENST00000644831.1:n.1897C=
ENST00000644933.1:c.*587C=	ENSP00000496133.1:n.*587C=
ENST00000645285.1:c.*587C=	ENSP00000495058.1:n.*587C=
ENST00000645331.1:n.2926C=
ENST00000645620.1:c.*29C=	ENSP00000493657.1:n.*29C=
ENST00000646691.1:n.1608C=
ENST00000646777.1:n.2054C=
ENST00000647016.1:n.2201C=
ENST00000647152.1:c.*29C=	ENSP00000495893.1:n.*29C=
ENST00000647209.1:c.*1590C=	ENSP00000495558.1:n.*1590C=
ENST00000647346.1:n.2741C=
ENST00000299427.10:c.*29C=	ENSP00000299427.6:n.*29C=
ENST00000533371.5:c.*29C=	ENSP00000437066.1:n.*29C=
ENST00000611494.4:c.*49C=	ENSP00000484546.1:n.*49C=
NM_000391.3:c.*29C=	NP_000382.3:n.*29C=
NM_000391.4:c.*29C= MANE Select	NP_000382.3:n.*29C=