Canonical Allele Identifier: CA1950232471

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614498T= , CM000673.2:g.6614498T=	GRCh38
NC_000011.9:g.6635729T= , CM000673.1:g.6635729T=	GRCh37
NC_000011.8:g.6592305T=	NCBI36
NG_008653.1:g.9964A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*48A=	ENSP00000507321.1:n.*48A=
ENST00000299427.12:c.*48A= MANE Select	ENSP00000299427.6:n.*48A=
ENST00000524611.2:n.779A=
ENST00000533371.6:c.*48A=	ENSP00000437066.1:n.*48A=
ENST00000642892.1:c.*48A=	ENSP00000494165.1:n.*48A=
ENST00000643342.1:c.813A=
ENST00000643439.1:c.*1480A=	ENSP00000495849.1:n.*1480A=
ENST00000643479.1:n.1926A=
ENST00000643516.1:c.1249A=
ENST00000644218.1:c.*48A=	ENSP00000493574.1:n.*48A=
ENST00000644683.1:c.*1193A=	ENSP00000494085.1:n.*1193A=
ENST00000644810.1:c.*48A=	ENSP00000495895.1:n.*48A=
ENST00000644831.1:n.1916A=
ENST00000644933.1:c.*606A=	ENSP00000496133.1:n.*606A=
ENST00000645285.1:c.*606A=	ENSP00000495058.1:n.*606A=
ENST00000645331.1:n.2945A=
ENST00000645620.1:c.*48A=	ENSP00000493657.1:n.*48A=
ENST00000646691.1:n.1627A=
ENST00000646777.1:n.2073A=
ENST00000647016.1:n.2220A=
ENST00000647152.1:c.*48A=	ENSP00000495893.1:n.*48A=
ENST00000647209.1:c.*1609A=	ENSP00000495558.1:n.*1609A=
ENST00000647346.1:n.2760A=
ENST00000299427.10:c.*48A=	ENSP00000299427.6:n.*48A=
ENST00000533371.5:c.*48A=	ENSP00000437066.1:n.*48A=
ENST00000611494.4:c.*68A=	ENSP00000484546.1:n.*68A=
NM_000391.3:c.*48A=	NP_000382.3:n.*48A=
NM_000391.4:c.*48A= MANE Select	NP_000382.3:n.*48A=