Canonical Allele Identifier: CA1950234242

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615329C= , CM000673.2:g.6615329C=	GRCh38
NC_000011.9:g.6636560C= , CM000673.1:g.6636560C=	GRCh37
NC_000011.8:g.6593136C=	NCBI36
NG_008653.1:g.9133G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1153G=	ENSP00000507321.1:p.Glu385=
ENST00000299427.12:c.1267G= MANE Select	ENSP00000299427.6:p.Glu423=
ENST00000436873.7:c.504G=
ENST00000524611.2:n.127G=
ENST00000524924.2:n.387G=
ENST00000533371.6:c.538G=	ENSP00000437066.1:p.Glu180=
ENST00000642892.1:c.538G=	ENSP00000494165.1:p.Glu180=
ENST00000643342.1:c.340G=
ENST00000643439.1:c.*1007G=	ENSP00000495849.1:n.*1007G=
ENST00000643479.1:n.1453G=
ENST00000643516.1:c.776G=
ENST00000644218.1:c.1078G=	ENSP00000493574.1:p.Glu360=
ENST00000644683.1:c.*720G=	ENSP00000494085.1:n.*720G=
ENST00000644810.1:c.988G=	ENSP00000495895.1:p.Glu330=
ENST00000644831.1:n.1443G=
ENST00000644933.1:c.*133G=	ENSP00000496133.1:n.*133G=
ENST00000645285.1:c.*133G=	ENSP00000495058.1:n.*133G=
ENST00000645331.1:n.2472G=
ENST00000645620.1:c.538G=	ENSP00000493657.1:p.Glu180=
ENST00000646691.1:n.1154G=
ENST00000646777.1:n.1600G=
ENST00000647016.1:n.1747G=
ENST00000647152.1:c.538G=	ENSP00000495893.1:p.Glu180=
ENST00000647209.1:c.*1136G=	ENSP00000495558.1:n.*1136G=
ENST00000647346.1:n.2287G=
ENST00000299427.10:c.1267G=	ENSP00000299427.6:p.Glu423=
ENST00000524611.1:n.145G=
ENST00000524924.1:n.222G=
ENST00000532191.1:n.320G=
ENST00000533371.5:c.538G=	ENSP00000437066.1:p.Glu180=
ENST00000611494.4:c.1267G=	ENSP00000484546.1:p.Glu423=
NM_000391.3:c.1267G=	NP_000382.3:p.Glu423=
NM_000391.4:c.1267G= MANE Select	NP_000382.3:p.Glu423=