Canonical Allele Identifier: CA1950234581

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615455C= , CM000673.2:g.6615455C=	GRCh38
NC_000011.9:g.6636686C= , CM000673.1:g.6636686C=	GRCh37
NC_000011.8:g.6593262C=	NCBI36
NG_008653.1:g.9007G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1139G=	ENSP00000507321.1:p.Arg380=
ENST00000299427.12:c.1253G= MANE Select	ENSP00000299427.6:p.Arg418=
ENST00000436873.7:c.490G=
ENST00000524611.2:n.1G=
ENST00000524924.2:n.373G=
ENST00000533371.6:c.524G=	ENSP00000437066.1:p.Arg175=
ENST00000642892.1:c.524G=	ENSP00000494165.1:p.Arg175=
ENST00000643342.1:c.326G=
ENST00000643439.1:c.*993G=	ENSP00000495849.1:n.*993G=
ENST00000643479.1:n.1439G=
ENST00000643516.1:c.762G=
ENST00000644218.1:c.1064G=	ENSP00000493574.1:p.Arg355=
ENST00000644683.1:c.*706G=	ENSP00000494085.1:n.*706G=
ENST00000644810.1:c.974G=	ENSP00000495895.1:p.Arg325=
ENST00000644831.1:n.1429G=
ENST00000644933.1:c.*119G=	ENSP00000496133.1:n.*119G=
ENST00000645285.1:c.*119G=	ENSP00000495058.1:n.*119G=
ENST00000645331.1:n.2458G=
ENST00000645620.1:c.524G=	ENSP00000493657.1:p.Arg175=
ENST00000646691.1:n.1028G=
ENST00000646777.1:n.1586G=
ENST00000647016.1:n.1733G=
ENST00000647152.1:c.524G=	ENSP00000495893.1:p.Arg175=
ENST00000647209.1:c.*1122G=	ENSP00000495558.1:n.*1122G=
ENST00000647346.1:n.2273G=
ENST00000299427.10:c.1253G=	ENSP00000299427.6:p.Arg418=
ENST00000524611.1:n.19G=
ENST00000524924.1:n.208G=
ENST00000532191.1:n.306G=
ENST00000533371.5:c.524G=	ENSP00000437066.1:p.Arg175=
ENST00000611494.4:c.1253G=	ENSP00000484546.1:p.Arg418=
NM_000391.3:c.1253G=	NP_000382.3:p.Arg418=
NM_000391.4:c.1253G= MANE Select	NP_000382.3:p.Arg418=