Canonical Allele Identifier: CA1950232442

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614479G= , CM000673.2:g.6614479G=	GRCh38
NC_000011.9:g.6635710G= , CM000673.1:g.6635710G=	GRCh37
NC_000011.8:g.6592286G=	NCBI36
NG_008653.1:g.9983C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*67C=	ENSP00000507321.1:n.*67C=
ENST00000299427.12:c.*67C= MANE Select	ENSP00000299427.6:n.*67C=
ENST00000524611.2:n.798C=
ENST00000533371.6:c.*67C=	ENSP00000437066.1:n.*67C=
ENST00000642892.1:c.*67C=	ENSP00000494165.1:n.*67C=
ENST00000643342.1:c.832C=
ENST00000643439.1:c.*1499C=	ENSP00000495849.1:n.*1499C=
ENST00000643479.1:n.1945C=
ENST00000643516.1:c.1268C=
ENST00000644218.1:c.*67C=	ENSP00000493574.1:n.*67C=
ENST00000644683.1:c.*1212C=	ENSP00000494085.1:n.*1212C=
ENST00000644810.1:c.*67C=	ENSP00000495895.1:n.*67C=
ENST00000644831.1:n.1935C=
ENST00000644933.1:c.*625C=	ENSP00000496133.1:n.*625C=
ENST00000645285.1:c.*625C=	ENSP00000495058.1:n.*625C=
ENST00000645331.1:n.2964C=
ENST00000645620.1:c.*67C=	ENSP00000493657.1:n.*67C=
ENST00000646691.1:n.1646C=
ENST00000646777.1:n.2092C=
ENST00000647016.1:n.2239C=
ENST00000647152.1:c.*67C=	ENSP00000495893.1:n.*67C=
ENST00000647209.1:c.*1628C=	ENSP00000495558.1:n.*1628C=
ENST00000647346.1:n.2779C=
ENST00000299427.10:c.*67C=	ENSP00000299427.6:n.*67C=
ENST00000533371.5:c.*67C=	ENSP00000437066.1:n.*67C=
ENST00000611494.4:c.*87C=	ENSP00000484546.1:n.*87C=
NM_000391.3:c.*67C=	NP_000382.3:n.*67C=
NM_000391.4:c.*67C= MANE Select	NP_000382.3:n.*67C=