Canonical Allele Identifier: CA1950235673

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616056C= , CM000673.2:g.6616056C=	GRCh38
NC_000011.9:g.6637287C= , CM000673.1:g.6637287C=	GRCh37
NC_000011.8:g.6593863C=	NCBI36
NG_008653.1:g.8406G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.980G=	ENSP00000507321.1:p.Cys327=
ENST00000299427.12:c.1094G= MANE Select	ENSP00000299427.6:p.Cys365=
ENST00000436873.7:c.331G=
ENST00000524924.2:n.214G=
ENST00000533371.6:c.365G=	ENSP00000437066.1:p.Cys122=
ENST00000642892.1:c.365G=	ENSP00000494165.1:p.Cys122=
ENST00000643342.1:c.184G=
ENST00000643439.1:c.*834G=	ENSP00000495849.1:n.*834G=
ENST00000643479.1:n.1280G=
ENST00000643516.1:c.603G=
ENST00000644218.1:c.905G=	ENSP00000493574.1:p.Cys302=
ENST00000644683.1:c.*547G=	ENSP00000494085.1:n.*547G=
ENST00000644810.1:c.815G=	ENSP00000495895.1:p.Cys272=
ENST00000644831.1:n.1270G=
ENST00000644933.1:c.365G=	ENSP00000496133.1:p.Cys122=
ENST00000645285.1:c.176G=	ENSP00000495058.1:p.Cys59=
ENST00000645331.1:n.1857G=
ENST00000645620.1:c.365G=	ENSP00000493657.1:p.Cys122=
ENST00000646691.1:n.427G=
ENST00000646777.1:n.1427G=
ENST00000647016.1:n.1574G=
ENST00000647152.1:c.365G=	ENSP00000495893.1:p.Cys122=
ENST00000647209.1:c.*963G=	ENSP00000495558.1:n.*963G=
ENST00000647346.1:n.2114G=
ENST00000299427.10:c.1094G=	ENSP00000299427.6:p.Cys365=
ENST00000524924.1:n.49G=
ENST00000533371.5:c.365G=	ENSP00000437066.1:p.Cys122=
ENST00000611494.4:c.1094G=	ENSP00000484546.1:p.Cys365=
NM_000391.3:c.1094G=	NP_000382.3:p.Cys365=
NM_000391.4:c.1094G= MANE Select	NP_000382.3:p.Cys365=