Canonical Allele Identifier: CA1950232438

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614477G= , CM000673.2:g.6614477G=	GRCh38
NC_000011.9:g.6635708G= , CM000673.1:g.6635708G=	GRCh37
NC_000011.8:g.6592284G=	NCBI36
NG_008653.1:g.9985C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*69C=	ENSP00000507321.1:n.*69C=
ENST00000299427.12:c.*69C= MANE Select	ENSP00000299427.6:n.*69C=
ENST00000524611.2:n.800C=
ENST00000533371.6:c.*69C=	ENSP00000437066.1:n.*69C=
ENST00000642892.1:c.*69C=	ENSP00000494165.1:n.*69C=
ENST00000643342.1:c.834C=
ENST00000643439.1:c.*1501C=	ENSP00000495849.1:n.*1501C=
ENST00000643479.1:n.1947C=
ENST00000643516.1:c.1270C=
ENST00000644218.1:c.*69C=	ENSP00000493574.1:n.*69C=
ENST00000644683.1:c.*1214C=	ENSP00000494085.1:n.*1214C=
ENST00000644810.1:c.*69C=	ENSP00000495895.1:n.*69C=
ENST00000644831.1:n.1937C=
ENST00000644933.1:c.*627C=	ENSP00000496133.1:n.*627C=
ENST00000645285.1:c.*627C=	ENSP00000495058.1:n.*627C=
ENST00000645331.1:n.2966C=
ENST00000645620.1:c.*69C=	ENSP00000493657.1:n.*69C=
ENST00000646691.1:n.1648C=
ENST00000646777.1:n.2094C=
ENST00000647016.1:n.2241C=
ENST00000647152.1:c.*69C=	ENSP00000495893.1:n.*69C=
ENST00000647209.1:c.*1630C=	ENSP00000495558.1:n.*1630C=
ENST00000647346.1:n.2781C=
ENST00000299427.10:c.*69C=	ENSP00000299427.6:n.*69C=
ENST00000533371.5:c.*69C=	ENSP00000437066.1:n.*69C=
ENST00000611494.4:c.*89C=	ENSP00000484546.1:n.*89C=
NM_000391.3:c.*69C=	NP_000382.3:n.*69C=
NM_000391.4:c.*69C= MANE Select	NP_000382.3:n.*69C=