Canonical Allele Identifier: CA1950232458

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614483A= , CM000673.2:g.6614483A=	GRCh38
NC_000011.9:g.6635714A= , CM000673.1:g.6635714A=	GRCh37
NC_000011.8:g.6592290A=	NCBI36
NG_008653.1:g.9979T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*63T=	ENSP00000507321.1:n.*63T=
ENST00000299427.12:c.*63T= MANE Select	ENSP00000299427.6:n.*63T=
ENST00000524611.2:n.794T=
ENST00000533371.6:c.*63T=	ENSP00000437066.1:n.*63T=
ENST00000642892.1:c.*63T=	ENSP00000494165.1:n.*63T=
ENST00000643342.1:c.828T=
ENST00000643439.1:c.*1495T=	ENSP00000495849.1:n.*1495T=
ENST00000643479.1:n.1941T=
ENST00000643516.1:c.1264T=
ENST00000644218.1:c.*63T=	ENSP00000493574.1:n.*63T=
ENST00000644683.1:c.*1208T=	ENSP00000494085.1:n.*1208T=
ENST00000644810.1:c.*63T=	ENSP00000495895.1:n.*63T=
ENST00000644831.1:n.1931T=
ENST00000644933.1:c.*621T=	ENSP00000496133.1:n.*621T=
ENST00000645285.1:c.*621T=	ENSP00000495058.1:n.*621T=
ENST00000645331.1:n.2960T=
ENST00000645620.1:c.*63T=	ENSP00000493657.1:n.*63T=
ENST00000646691.1:n.1642T=
ENST00000646777.1:n.2088T=
ENST00000647016.1:n.2235T=
ENST00000647152.1:c.*63T=	ENSP00000495893.1:n.*63T=
ENST00000647209.1:c.*1624T=	ENSP00000495558.1:n.*1624T=
ENST00000647346.1:n.2775T=
ENST00000299427.10:c.*63T=	ENSP00000299427.6:n.*63T=
ENST00000533371.5:c.*63T=	ENSP00000437066.1:n.*63T=
ENST00000611494.4:c.*83T=	ENSP00000484546.1:n.*83T=
NM_000391.3:c.*63T=	NP_000382.3:n.*63T=
NM_000391.4:c.*63T= MANE Select	NP_000382.3:n.*63T=