Canonical Allele Identifier: CA1950232498

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614516G= , CM000673.2:g.6614516G=	GRCh38
NC_000011.9:g.6635747G= , CM000673.1:g.6635747G=	GRCh37
NC_000011.8:g.6592323G=	NCBI36
NG_008653.1:g.9946C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*30C=	ENSP00000507321.1:n.*30C=
ENST00000299427.12:c.*30C= MANE Select	ENSP00000299427.6:n.*30C=
ENST00000524611.2:n.761C=
ENST00000533371.6:c.*30C=	ENSP00000437066.1:n.*30C=
ENST00000642892.1:c.*30C=	ENSP00000494165.1:n.*30C=
ENST00000643342.1:c.795C=
ENST00000643439.1:c.*1462C=	ENSP00000495849.1:n.*1462C=
ENST00000643479.1:n.1908C=
ENST00000643516.1:c.1231C=
ENST00000644218.1:c.*30C=	ENSP00000493574.1:n.*30C=
ENST00000644683.1:c.*1175C=	ENSP00000494085.1:n.*1175C=
ENST00000644810.1:c.*30C=	ENSP00000495895.1:n.*30C=
ENST00000644831.1:n.1898C=
ENST00000644933.1:c.*588C=	ENSP00000496133.1:n.*588C=
ENST00000645285.1:c.*588C=	ENSP00000495058.1:n.*588C=
ENST00000645331.1:n.2927C=
ENST00000645620.1:c.*30C=	ENSP00000493657.1:n.*30C=
ENST00000646691.1:n.1609C=
ENST00000646777.1:n.2055C=
ENST00000647016.1:n.2202C=
ENST00000647152.1:c.*30C=	ENSP00000495893.1:n.*30C=
ENST00000647209.1:c.*1591C=	ENSP00000495558.1:n.*1591C=
ENST00000647346.1:n.2742C=
ENST00000299427.10:c.*30C=	ENSP00000299427.6:n.*30C=
ENST00000533371.5:c.*30C=	ENSP00000437066.1:n.*30C=
ENST00000611494.4:c.*50C=	ENSP00000484546.1:n.*50C=
NM_000391.3:c.*30C=	NP_000382.3:n.*30C=
NM_000391.4:c.*30C= MANE Select	NP_000382.3:n.*30C=