Canonical Allele Identifier: CA1950214890

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617354C= , CM000673.2:g.6617354C=	GRCh38
NC_000011.9:g.6638585C= , CM000673.1:g.6638585C=	GRCh37
NC_000011.8:g.6595161C=	NCBI36
NG_008653.1:g.7108G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.341G=	ENSP00000507321.1:p.Arg114=
ENST00000299427.12:c.455G= MANE Select	ENSP00000299427.6:p.Arg152=
ENST00000428886.7:n.543G=
ENST00000436873.7:c.259G=
ENST00000524788.2:n.1467G=
ENST00000524903.2:n.1583G=
ENST00000528571.6:c.*195G=	ENSP00000434647.1:n.*195G=
ENST00000528807.2:n.111G=
ENST00000530040.2:n.479+5G=
ENST00000533371.6:c.-275G=	ENSP00000437066.1:n.-275G=
ENST00000534644.6:n.456G=
ENST00000642892.1:c.-222G=	ENSP00000494165.1:n.-222G=
ENST00000643439.1:c.*195G=	ENSP00000495849.1:n.*195G=
ENST00000643479.1:n.484G=
ENST00000643516.1:c.342G=
ENST00000644151.1:n.1747G=
ENST00000644218.1:c.455G=	ENSP00000493574.1:p.Arg152=
ENST00000644683.1:c.450+5G=	ENSP00000494085.1:n.450+5G=
ENST00000644810.1:c.230-201G=	ENSP00000495895.1:n.230-201G=
ENST00000644831.1:n.484G=
ENST00000644933.1:c.-275G=	ENSP00000496133.1:n.-275G=
ENST00000645020.1:n.1483G=
ENST00000645285.1:c.-275G=	ENSP00000495058.1:n.-275G=
ENST00000645331.1:n.674G=
ENST00000645620.1:c.-222+5G=	ENSP00000493657.1:n.-222+5G=
ENST00000646777.1:n.484G=
ENST00000647016.1:n.788G=
ENST00000647152.1:c.-275G=	ENSP00000495893.1:n.-275G=
ENST00000647209.1:c.*324G=	ENSP00000495558.1:n.*324G=
ENST00000647346.1:n.1475G=
ENST00000299427.10:c.455G=	ENSP00000299427.6:p.Arg152=
ENST00000428886.6:n.477G=
ENST00000436873.6:c.450+5G=	ENSP00000398136.2:n.450+5G=
ENST00000524788.1:n.8G=
ENST00000528571.5:c.*195G=	ENSP00000434647.1:n.*195G=
ENST00000533371.5:c.-275G=	ENSP00000437066.1:n.-275G=
ENST00000534644.5:n.440G=
ENST00000611494.4:c.455G=	ENSP00000484546.1:p.Arg152=
NM_000391.3:c.455G=	NP_000382.3:p.Arg152=
NM_000391.4:c.455G= MANE Select	NP_000382.3:p.Arg152=