Canonical Allele Identifier: CA1950236268

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616332G= , CM000673.2:g.6616332G=	GRCh38
NC_000011.9:g.6637563G= , CM000673.1:g.6637563G=	GRCh37
NC_000011.8:g.6594139G=	NCBI36
NG_008653.1:g.8130C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.944C=	ENSP00000507321.1:p.Thr315=
ENST00000299427.12:c.1058C= MANE Select	ENSP00000299427.6:p.Thr353=
ENST00000436873.7:c.313-258C=
ENST00000533371.6:c.329C=	ENSP00000437066.1:p.Thr110=
ENST00000642892.1:c.329C=	ENSP00000494165.1:p.Thr110=
ENST00000643342.1:c.148C=
ENST00000643439.1:c.*798C=	ENSP00000495849.1:n.*798C=
ENST00000643479.1:n.1244C=
ENST00000643516.1:c.567C=
ENST00000644218.1:c.887-258C=	ENSP00000493574.1:n.887-258C=
ENST00000644683.1:c.*511C=	ENSP00000494085.1:n.*511C=
ENST00000644810.1:c.779C=	ENSP00000495895.1:p.Thr260=
ENST00000644831.1:n.1234C=
ENST00000644933.1:c.329C=	ENSP00000496133.1:p.Thr110=
ENST00000645285.1:c.158-258C=	ENSP00000495058.1:n.158-258C=
ENST00000645331.1:n.1581C=
ENST00000645620.1:c.329C=	ENSP00000493657.1:p.Thr110=
ENST00000646691.1:n.151C=
ENST00000646777.1:n.1391C=
ENST00000647016.1:n.1538C=
ENST00000647152.1:c.329C=	ENSP00000495893.1:p.Thr110=
ENST00000647209.1:c.*927C=	ENSP00000495558.1:n.*927C=
ENST00000647346.1:n.2078C=
ENST00000299427.10:c.1058C=	ENSP00000299427.6:p.Thr353=
ENST00000533371.5:c.329C=	ENSP00000437066.1:p.Thr110=
ENST00000611494.4:c.1058C=	ENSP00000484546.1:p.Thr353=
NM_000391.3:c.1058C=	NP_000382.3:p.Thr353=
NM_000391.4:c.1058C= MANE Select	NP_000382.3:p.Thr353=