Canonical Allele Identifier: CA1950234073

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615256C= , CM000673.2:g.6615256C=	GRCh38
NC_000011.9:g.6636487C= , CM000673.1:g.6636487C=	GRCh37
NC_000011.8:g.6593063C=	NCBI36
NG_008653.1:g.9206G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1226G=	ENSP00000507321.1:p.Arg409=
ENST00000299427.12:c.1340G= MANE Select	ENSP00000299427.6:p.Arg447=
ENST00000524611.2:n.200G=
ENST00000524924.2:n.460G=
ENST00000533371.6:c.611G=	ENSP00000437066.1:p.Arg204=
ENST00000642892.1:c.611G=	ENSP00000494165.1:p.Arg204=
ENST00000643342.1:c.413G=
ENST00000643439.1:c.*1080G=	ENSP00000495849.1:n.*1080G=
ENST00000643479.1:n.1526G=
ENST00000643516.1:c.849G=
ENST00000644218.1:c.1151G=	ENSP00000493574.1:p.Arg384=
ENST00000644683.1:c.*793G=	ENSP00000494085.1:n.*793G=
ENST00000644810.1:c.1061G=	ENSP00000495895.1:p.Arg354=
ENST00000644831.1:n.1516G=
ENST00000644933.1:c.*206G=	ENSP00000496133.1:n.*206G=
ENST00000645285.1:c.*206G=	ENSP00000495058.1:n.*206G=
ENST00000645331.1:n.2545G=
ENST00000645620.1:c.611G=	ENSP00000493657.1:p.Arg204=
ENST00000646691.1:n.1227G=
ENST00000646777.1:n.1673G=
ENST00000647016.1:n.1820G=
ENST00000647152.1:c.611G=	ENSP00000495893.1:p.Arg204=
ENST00000647209.1:c.*1209G=	ENSP00000495558.1:n.*1209G=
ENST00000647346.1:n.2360G=
ENST00000299427.10:c.1340G=	ENSP00000299427.6:p.Arg447=
ENST00000524611.1:n.218G=
ENST00000532191.1:n.393G=
ENST00000533371.5:c.611G=	ENSP00000437066.1:p.Arg204=
ENST00000611494.4:c.1340G=	ENSP00000484546.1:p.Arg447=
NM_000391.3:c.1340G=	NP_000382.3:p.Arg447=
NM_000391.4:c.1340G= MANE Select	NP_000382.3:p.Arg447=