Canonical Allele Identifier: CA1950236047

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616217G= , CM000673.2:g.6616217G=	GRCh38
NC_000011.9:g.6637448G= , CM000673.1:g.6637448G=	GRCh37
NC_000011.8:g.6594024G=	NCBI36
NG_008653.1:g.8245C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.961+98C=	ENSP00000507321.1:n.961+98C=
ENST00000299427.12:c.1075+98C= MANE Select	ENSP00000299427.6:n.1075+98C=
ENST00000436873.7:c.313-143C=
ENST00000524924.2:n.53C=
ENST00000533371.6:c.346+98C=	ENSP00000437066.1:n.346+98C=
ENST00000642892.1:c.346+98C=	ENSP00000494165.1:n.346+98C=
ENST00000643342.1:c.165+98C=
ENST00000643439.1:c.*815+98C=	ENSP00000495849.1:n.*815+98C=
ENST00000643479.1:n.1261+98C=
ENST00000643516.1:c.584+98C=
ENST00000644218.1:c.887-143C=	ENSP00000493574.1:n.887-143C=
ENST00000644683.1:c.*528+98C=	ENSP00000494085.1:n.*528+98C=
ENST00000644810.1:c.796+98C=	ENSP00000495895.1:n.796+98C=
ENST00000644831.1:n.1251+98C=
ENST00000644933.1:c.346+98C=	ENSP00000496133.1:n.346+98C=
ENST00000645285.1:c.158-143C=	ENSP00000495058.1:n.158-143C=
ENST00000645331.1:n.1696C=
ENST00000645620.1:c.346+98C=	ENSP00000493657.1:n.346+98C=
ENST00000646691.1:n.266C=
ENST00000646777.1:n.1408+98C=
ENST00000647016.1:n.1555+98C=
ENST00000647152.1:c.346+98C=	ENSP00000495893.1:n.346+98C=
ENST00000647209.1:c.*944+98C=	ENSP00000495558.1:n.*944+98C=
ENST00000647346.1:n.2095+98C=
ENST00000299427.10:c.1075+98C=	ENSP00000299427.6:n.1075+98C=
ENST00000533371.5:c.346+98C=	ENSP00000437066.1:n.346+98C=
ENST00000611494.4:c.1075+98C=	ENSP00000484546.1:n.1075+98C=
NM_000391.3:c.1075+98C=	NP_000382.3:n.1075+98C=
NM_000391.4:c.1075+98C= MANE Select	NP_000382.3:n.1075+98C=