Canonical Allele Identifier: CA1950237776

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617017G= , CM000673.2:g.6617017G=	GRCh38
NC_000011.9:g.6638248G= , CM000673.1:g.6638248G=	GRCh37
NC_000011.8:g.6594824G=	NCBI36
NG_008653.1:g.7445C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.531C=	ENSP00000507321.1:p.Asp177=
ENST00000299427.12:c.645C= MANE Select	ENSP00000299427.6:p.Asp215=
ENST00000436873.7:c.312+284C=
ENST00000524788.2:n.1804C=
ENST00000524903.2:n.1920C=
ENST00000528807.2:n.301C=
ENST00000530040.2:n.479+342C=
ENST00000533371.6:c.-85C=	ENSP00000437066.1:n.-85C=
ENST00000534644.6:n.593C=
ENST00000642892.1:c.-85C=	ENSP00000494165.1:n.-85C=
ENST00000643439.1:c.*385C=	ENSP00000495849.1:n.*385C=
ENST00000643479.1:n.674C=
ENST00000643516.1:c.395+284C=
ENST00000644151.1:n.2084C=
ENST00000644218.1:c.645C=	ENSP00000493574.1:p.Asp215=
ENST00000644683.1:c.*98C=	ENSP00000494085.1:n.*98C=
ENST00000644810.1:c.366C=	ENSP00000495895.1:p.Asp122=
ENST00000644831.1:n.821C=
ENST00000644933.1:c.-85C=	ENSP00000496133.1:n.-85C=
ENST00000645020.1:n.1820C=
ENST00000645285.1:c.-85C=	ENSP00000495058.1:n.-85C=
ENST00000645331.1:n.1011C=
ENST00000645620.1:c.-85C=	ENSP00000493657.1:n.-85C=
ENST00000646777.1:n.821C=
ENST00000647016.1:n.1125C=
ENST00000647152.1:c.-85C=	ENSP00000495893.1:n.-85C=
ENST00000647209.1:c.*514C=	ENSP00000495558.1:n.*514C=
ENST00000647346.1:n.1665C=
ENST00000299427.10:c.645C=	ENSP00000299427.6:p.Asp215=
ENST00000428886.6:n.814C=
ENST00000436873.6:c.450+342C=	ENSP00000398136.2:n.450+342C=
ENST00000524788.1:n.345C=
ENST00000528571.5:c.*385C=	ENSP00000434647.1:n.*385C=
ENST00000528807.1:n.195C=
ENST00000533371.5:c.-85C=	ENSP00000437066.1:n.-85C=
ENST00000534644.5:n.630C=
ENST00000611494.4:c.645C=	ENSP00000484546.1:p.Asp215=
NM_000391.3:c.645C=	NP_000382.3:p.Asp215=
NM_000391.4:c.645C= MANE Select	NP_000382.3:p.Asp215=