Canonical Allele Identifier: CA1950237901

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617057G= , CM000673.2:g.6617057G=	GRCh38
NC_000011.9:g.6638288G= , CM000673.1:g.6638288G=	GRCh37
NC_000011.8:g.6594864G=	NCBI36
NG_008653.1:g.7405C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.491C=	ENSP00000507321.1:p.Pro164=
ENST00000299427.12:c.605C= MANE Select	ENSP00000299427.6:p.Pro202=
ENST00000436873.7:c.312+244C=
ENST00000524788.2:n.1764C=
ENST00000524903.2:n.1880C=
ENST00000528807.2:n.261C=
ENST00000530040.2:n.479+302C=
ENST00000533371.6:c.-125C=	ENSP00000437066.1:n.-125C=
ENST00000534644.6:n.553C=
ENST00000642892.1:c.-125C=	ENSP00000494165.1:n.-125C=
ENST00000643439.1:c.*345C=	ENSP00000495849.1:n.*345C=
ENST00000643479.1:n.634C=
ENST00000643516.1:c.395+244C=
ENST00000644151.1:n.2044C=
ENST00000644218.1:c.605C=	ENSP00000493574.1:p.Pro202=
ENST00000644683.1:c.*58C=	ENSP00000494085.1:n.*58C=
ENST00000644810.1:c.326C=	ENSP00000495895.1:p.Pro109=
ENST00000644831.1:n.781C=
ENST00000644933.1:c.-125C=	ENSP00000496133.1:n.-125C=
ENST00000645020.1:n.1780C=
ENST00000645285.1:c.-125C=	ENSP00000495058.1:n.-125C=
ENST00000645331.1:n.971C=
ENST00000645620.1:c.-125C=	ENSP00000493657.1:n.-125C=
ENST00000646777.1:n.781C=
ENST00000647016.1:n.1085C=
ENST00000647152.1:c.-125C=	ENSP00000495893.1:n.-125C=
ENST00000647209.1:c.*474C=	ENSP00000495558.1:n.*474C=
ENST00000647346.1:n.1625C=
ENST00000299427.10:c.605C=	ENSP00000299427.6:p.Pro202=
ENST00000428886.6:n.774C=
ENST00000436873.6:c.450+302C=	ENSP00000398136.2:n.450+302C=
ENST00000524788.1:n.305C=
ENST00000528571.5:c.*345C=	ENSP00000434647.1:n.*345C=
ENST00000528807.1:n.155C=
ENST00000533371.5:c.-125C=	ENSP00000437066.1:n.-125C=
ENST00000534644.5:n.590C=
ENST00000611494.4:c.605C=	ENSP00000484546.1:p.Pro202=
NM_000391.3:c.605C=	NP_000382.3:p.Pro202=
NM_000391.4:c.605C= MANE Select	NP_000382.3:p.Pro202=