Canonical Allele Identifier: CA1950232420

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614468C= , CM000673.2:g.6614468C=	GRCh38
NC_000011.9:g.6635699C= , CM000673.1:g.6635699C=	GRCh37
NC_000011.8:g.6592275C=	NCBI36
NG_008653.1:g.9994G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*78G=	ENSP00000507321.1:n.*78G=
ENST00000299427.12:c.*78G= MANE Select	ENSP00000299427.6:n.*78G=
ENST00000524611.2:n.809G=
ENST00000533371.6:c.*78G=	ENSP00000437066.1:n.*78G=
ENST00000642892.1:c.*78G=	ENSP00000494165.1:n.*78G=
ENST00000643342.1:c.843G=
ENST00000643439.1:c.*1510G=	ENSP00000495849.1:n.*1510G=
ENST00000643479.1:n.1956G=
ENST00000643516.1:c.1279G=
ENST00000644218.1:c.*78G=	ENSP00000493574.1:n.*78G=
ENST00000644683.1:c.*1223G=	ENSP00000494085.1:n.*1223G=
ENST00000644810.1:c.*78G=	ENSP00000495895.1:n.*78G=
ENST00000644831.1:n.1946G=
ENST00000644933.1:c.*636G=	ENSP00000496133.1:n.*636G=
ENST00000645285.1:c.*636G=	ENSP00000495058.1:n.*636G=
ENST00000645331.1:n.2975G=
ENST00000645620.1:c.*78G=	ENSP00000493657.1:n.*78G=
ENST00000646691.1:n.1657G=
ENST00000646777.1:n.2103G=
ENST00000647016.1:n.2250G=
ENST00000647152.1:c.*78G=	ENSP00000495893.1:n.*78G=
ENST00000647209.1:c.*1639G=	ENSP00000495558.1:n.*1639G=
ENST00000647346.1:n.2790G=
ENST00000299427.10:c.*78G=	ENSP00000299427.6:n.*78G=
ENST00000533371.5:c.*78G=	ENSP00000437066.1:n.*78G=
ENST00000611494.4:c.*98G=	ENSP00000484546.1:n.*98G=
NM_000391.3:c.*78G=	NP_000382.3:n.*78G=
NM_000391.4:c.*78G= MANE Select	NP_000382.3:n.*78G=