Canonical Allele Identifier: CA1950232431

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614475C= , CM000673.2:g.6614475C=	GRCh38
NC_000011.9:g.6635706C= , CM000673.1:g.6635706C=	GRCh37
NC_000011.8:g.6592282C=	NCBI36
NG_008653.1:g.9987G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*71G=	ENSP00000507321.1:n.*71G=
ENST00000299427.12:c.*71G= MANE Select	ENSP00000299427.6:n.*71G=
ENST00000524611.2:n.802G=
ENST00000533371.6:c.*71G=	ENSP00000437066.1:n.*71G=
ENST00000642892.1:c.*71G=	ENSP00000494165.1:n.*71G=
ENST00000643342.1:c.836G=
ENST00000643439.1:c.*1503G=	ENSP00000495849.1:n.*1503G=
ENST00000643479.1:n.1949G=
ENST00000643516.1:c.1272G=
ENST00000644218.1:c.*71G=	ENSP00000493574.1:n.*71G=
ENST00000644683.1:c.*1216G=	ENSP00000494085.1:n.*1216G=
ENST00000644810.1:c.*71G=	ENSP00000495895.1:n.*71G=
ENST00000644831.1:n.1939G=
ENST00000644933.1:c.*629G=	ENSP00000496133.1:n.*629G=
ENST00000645285.1:c.*629G=	ENSP00000495058.1:n.*629G=
ENST00000645331.1:n.2968G=
ENST00000645620.1:c.*71G=	ENSP00000493657.1:n.*71G=
ENST00000646691.1:n.1650G=
ENST00000646777.1:n.2096G=
ENST00000647016.1:n.2243G=
ENST00000647152.1:c.*71G=	ENSP00000495893.1:n.*71G=
ENST00000647209.1:c.*1632G=	ENSP00000495558.1:n.*1632G=
ENST00000647346.1:n.2783G=
ENST00000299427.10:c.*71G=	ENSP00000299427.6:n.*71G=
ENST00000533371.5:c.*71G=	ENSP00000437066.1:n.*71G=
ENST00000611494.4:c.*91G=	ENSP00000484546.1:n.*91G=
NM_000391.3:c.*71G=	NP_000382.3:n.*71G=
NM_000391.4:c.*71G= MANE Select	NP_000382.3:n.*71G=