Canonical Allele Identifier: CA1950232466

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614487A= , CM000673.2:g.6614487A=	GRCh38
NC_000011.9:g.6635718A= , CM000673.1:g.6635718A=	GRCh37
NC_000011.8:g.6592294A=	NCBI36
NG_008653.1:g.9975T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*59T=	ENSP00000507321.1:n.*59T=
ENST00000299427.12:c.*59T= MANE Select	ENSP00000299427.6:n.*59T=
ENST00000524611.2:n.790T=
ENST00000533371.6:c.*59T=	ENSP00000437066.1:n.*59T=
ENST00000642892.1:c.*59T=	ENSP00000494165.1:n.*59T=
ENST00000643342.1:c.824T=
ENST00000643439.1:c.*1491T=	ENSP00000495849.1:n.*1491T=
ENST00000643479.1:n.1937T=
ENST00000643516.1:c.1260T=
ENST00000644218.1:c.*59T=	ENSP00000493574.1:n.*59T=
ENST00000644683.1:c.*1204T=	ENSP00000494085.1:n.*1204T=
ENST00000644810.1:c.*59T=	ENSP00000495895.1:n.*59T=
ENST00000644831.1:n.1927T=
ENST00000644933.1:c.*617T=	ENSP00000496133.1:n.*617T=
ENST00000645285.1:c.*617T=	ENSP00000495058.1:n.*617T=
ENST00000645331.1:n.2956T=
ENST00000645620.1:c.*59T=	ENSP00000493657.1:n.*59T=
ENST00000646691.1:n.1638T=
ENST00000646777.1:n.2084T=
ENST00000647016.1:n.2231T=
ENST00000647152.1:c.*59T=	ENSP00000495893.1:n.*59T=
ENST00000647209.1:c.*1620T=	ENSP00000495558.1:n.*1620T=
ENST00000647346.1:n.2771T=
ENST00000299427.10:c.*59T=	ENSP00000299427.6:n.*59T=
ENST00000533371.5:c.*59T=	ENSP00000437066.1:n.*59T=
ENST00000611494.4:c.*79T=	ENSP00000484546.1:n.*79T=
NM_000391.3:c.*59T=	NP_000382.3:n.*59T=
NM_000391.4:c.*59T= MANE Select	NP_000382.3:n.*59T=