Canonical Allele Identifier: CA1950234701

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615517G= , CM000673.2:g.6615517G=	GRCh38
NC_000011.9:g.6636748G= , CM000673.1:g.6636748G=	GRCh37
NC_000011.8:g.6593324G=	NCBI36
NG_008653.1:g.8945C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1077C=	ENSP00000507321.1:p.Phe359=
ENST00000299427.12:c.1191C= MANE Select	ENSP00000299427.6:p.Phe397=
ENST00000436873.7:c.428C=
ENST00000524924.2:n.311C=
ENST00000533371.6:c.462C=	ENSP00000437066.1:p.Phe154=
ENST00000642892.1:c.462C=	ENSP00000494165.1:p.Phe154=
ENST00000643342.1:c.264C=
ENST00000643439.1:c.*931C=	ENSP00000495849.1:n.*931C=
ENST00000643479.1:n.1377C=
ENST00000643516.1:c.700C=
ENST00000644218.1:c.1002C=	ENSP00000493574.1:p.Phe334=
ENST00000644683.1:c.*644C=	ENSP00000494085.1:n.*644C=
ENST00000644810.1:c.912C=	ENSP00000495895.1:p.Phe304=
ENST00000644831.1:n.1367C=
ENST00000644933.1:c.*57C=	ENSP00000496133.1:n.*57C=
ENST00000645285.1:c.*57C=	ENSP00000495058.1:n.*57C=
ENST00000645331.1:n.2396C=
ENST00000645620.1:c.462C=	ENSP00000493657.1:p.Phe154=
ENST00000646691.1:n.966C=
ENST00000646777.1:n.1524C=
ENST00000647016.1:n.1671C=
ENST00000647152.1:c.462C=	ENSP00000495893.1:p.Phe154=
ENST00000647209.1:c.*1060C=	ENSP00000495558.1:n.*1060C=
ENST00000647346.1:n.2211C=
ENST00000299427.10:c.1191C=	ENSP00000299427.6:p.Phe397=
ENST00000524924.1:n.146C=
ENST00000532191.1:n.244C=
ENST00000533371.5:c.462C=	ENSP00000437066.1:p.Phe154=
ENST00000611494.4:c.1191C=	ENSP00000484546.1:p.Phe397=
NM_000391.3:c.1191C=	NP_000382.3:p.Phe397=
NM_000391.4:c.1191C= MANE Select	NP_000382.3:p.Phe397=