Canonical Allele Identifier: CA1950234577

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615453G= , CM000673.2:g.6615453G=	GRCh38
NC_000011.9:g.6636684G= , CM000673.1:g.6636684G=	GRCh37
NC_000011.8:g.6593260G=	NCBI36
NG_008653.1:g.9009C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1141C=	ENSP00000507321.1:p.Pro381=
ENST00000299427.12:c.1255C= MANE Select	ENSP00000299427.6:p.Pro419=
ENST00000436873.7:c.492C=
ENST00000524611.2:n.3C=
ENST00000524924.2:n.375C=
ENST00000533371.6:c.526C=	ENSP00000437066.1:p.Pro176=
ENST00000642892.1:c.526C=	ENSP00000494165.1:p.Pro176=
ENST00000643342.1:c.328C=
ENST00000643439.1:c.*995C=	ENSP00000495849.1:n.*995C=
ENST00000643479.1:n.1441C=
ENST00000643516.1:c.764C=
ENST00000644218.1:c.1066C=	ENSP00000493574.1:p.Pro356=
ENST00000644683.1:c.*708C=	ENSP00000494085.1:n.*708C=
ENST00000644810.1:c.976C=	ENSP00000495895.1:p.Pro326=
ENST00000644831.1:n.1431C=
ENST00000644933.1:c.*121C=	ENSP00000496133.1:n.*121C=
ENST00000645285.1:c.*121C=	ENSP00000495058.1:n.*121C=
ENST00000645331.1:n.2460C=
ENST00000645620.1:c.526C=	ENSP00000493657.1:p.Pro176=
ENST00000646691.1:n.1030C=
ENST00000646777.1:n.1588C=
ENST00000647016.1:n.1735C=
ENST00000647152.1:c.526C=	ENSP00000495893.1:p.Pro176=
ENST00000647209.1:c.*1124C=	ENSP00000495558.1:n.*1124C=
ENST00000647346.1:n.2275C=
ENST00000299427.10:c.1255C=	ENSP00000299427.6:p.Pro419=
ENST00000524611.1:n.21C=
ENST00000524924.1:n.210C=
ENST00000532191.1:n.308C=
ENST00000533371.5:c.526C=	ENSP00000437066.1:p.Pro176=
ENST00000611494.4:c.1255C=	ENSP00000484546.1:p.Pro419=
NM_000391.3:c.1255C=	NP_000382.3:p.Pro419=
NM_000391.4:c.1255C= MANE Select	NP_000382.3:p.Pro419=