Canonical Allele Identifier: CA1950234711

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615522G= , CM000673.2:g.6615522G=	GRCh38
NC_000011.9:g.6636753G= , CM000673.1:g.6636753G=	GRCh37
NC_000011.8:g.6593329G=	NCBI36
NG_008653.1:g.8940C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1072C=	ENSP00000507321.1:p.Pro358=
ENST00000299427.12:c.1186C= MANE Select	ENSP00000299427.6:p.Pro396=
ENST00000436873.7:c.423C=
ENST00000524924.2:n.306C=
ENST00000533371.6:c.457C=	ENSP00000437066.1:p.Pro153=
ENST00000642892.1:c.457C=	ENSP00000494165.1:p.Pro153=
ENST00000643342.1:c.259C=
ENST00000643439.1:c.*926C=	ENSP00000495849.1:n.*926C=
ENST00000643479.1:n.1372C=
ENST00000643516.1:c.695C=
ENST00000644218.1:c.997C=	ENSP00000493574.1:p.Pro333=
ENST00000644683.1:c.*639C=	ENSP00000494085.1:n.*639C=
ENST00000644810.1:c.907C=	ENSP00000495895.1:p.Pro303=
ENST00000644831.1:n.1362C=
ENST00000644933.1:c.*52C=	ENSP00000496133.1:n.*52C=
ENST00000645285.1:c.*52C=	ENSP00000495058.1:n.*52C=
ENST00000645331.1:n.2391C=
ENST00000645620.1:c.457C=	ENSP00000493657.1:p.Pro153=
ENST00000646691.1:n.961C=
ENST00000646777.1:n.1519C=
ENST00000647016.1:n.1666C=
ENST00000647152.1:c.457C=	ENSP00000495893.1:p.Pro153=
ENST00000647209.1:c.*1055C=	ENSP00000495558.1:n.*1055C=
ENST00000647346.1:n.2206C=
ENST00000299427.10:c.1186C=	ENSP00000299427.6:p.Pro396=
ENST00000524924.1:n.141C=
ENST00000532191.1:n.239C=
ENST00000533371.5:c.457C=	ENSP00000437066.1:p.Pro153=
ENST00000611494.4:c.1186C=	ENSP00000484546.1:p.Pro396=
NM_000391.3:c.1186C=	NP_000382.3:p.Pro396=
NM_000391.4:c.1186C= MANE Select	NP_000382.3:p.Pro396=