Canonical Allele Identifier: CA1950235720

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616063C= , CM000673.2:g.6616063C=	GRCh38
NC_000011.9:g.6637294C= , CM000673.1:g.6637294C=	GRCh37
NC_000011.8:g.6593870C=	NCBI36
NG_008653.1:g.8399G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.973G=	ENSP00000507321.1:p.Ala325=
ENST00000299427.12:c.1087G= MANE Select	ENSP00000299427.6:p.Ala363=
ENST00000436873.7:c.324G=
ENST00000524924.2:n.207G=
ENST00000533371.6:c.358G=	ENSP00000437066.1:p.Ala120=
ENST00000642892.1:c.358G=	ENSP00000494165.1:p.Ala120=
ENST00000643342.1:c.177G=
ENST00000643439.1:c.*827G=	ENSP00000495849.1:n.*827G=
ENST00000643479.1:n.1273G=
ENST00000643516.1:c.596G=
ENST00000644218.1:c.898G=	ENSP00000493574.1:p.Ala300=
ENST00000644683.1:c.*540G=	ENSP00000494085.1:n.*540G=
ENST00000644810.1:c.808G=	ENSP00000495895.1:p.Ala270=
ENST00000644831.1:n.1263G=
ENST00000644933.1:c.358G=	ENSP00000496133.1:p.Ala120=
ENST00000645285.1:c.169G=	ENSP00000495058.1:p.Ala57=
ENST00000645331.1:n.1850G=
ENST00000645620.1:c.358G=	ENSP00000493657.1:p.Ala120=
ENST00000646691.1:n.420G=
ENST00000646777.1:n.1420G=
ENST00000647016.1:n.1567G=
ENST00000647152.1:c.358G=	ENSP00000495893.1:p.Ala120=
ENST00000647209.1:c.*956G=	ENSP00000495558.1:n.*956G=
ENST00000647346.1:n.2107G=
ENST00000299427.10:c.1087G=	ENSP00000299427.6:p.Ala363=
ENST00000524924.1:n.42G=
ENST00000533371.5:c.358G=	ENSP00000437066.1:p.Ala120=
ENST00000611494.4:c.1087G=	ENSP00000484546.1:p.Ala363=
NM_000391.3:c.1087G=	NP_000382.3:p.Ala363=
NM_000391.4:c.1087G= MANE Select	NP_000382.3:p.Ala363=