Canonical Allele Identifier: CA1950233948

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615204G= , CM000673.2:g.6615204G=	GRCh38
NC_000011.9:g.6636435G= , CM000673.1:g.6636435G=	GRCh37
NC_000011.8:g.6593011G=	NCBI36
NG_008653.1:g.9258C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1278C=	ENSP00000507321.1:p.Asn426=
ENST00000299427.12:c.1392C= MANE Select	ENSP00000299427.6:p.Asn464=
ENST00000524611.2:n.252C=
ENST00000524924.2:n.512C=
ENST00000533371.6:c.663C=	ENSP00000437066.1:p.Asn221=
ENST00000642892.1:c.663C=	ENSP00000494165.1:p.Asn221=
ENST00000643342.1:c.465C=
ENST00000643439.1:c.*1132C=	ENSP00000495849.1:n.*1132C=
ENST00000643479.1:n.1578C=
ENST00000643516.1:c.901C=
ENST00000644218.1:c.1203C=	ENSP00000493574.1:p.Asn401=
ENST00000644683.1:c.*845C=	ENSP00000494085.1:n.*845C=
ENST00000644810.1:c.1113C=	ENSP00000495895.1:p.Asn371=
ENST00000644831.1:n.1568C=
ENST00000644933.1:c.*258C=	ENSP00000496133.1:n.*258C=
ENST00000645285.1:c.*258C=	ENSP00000495058.1:n.*258C=
ENST00000645331.1:n.2597C=
ENST00000645620.1:c.663C=	ENSP00000493657.1:p.Asn221=
ENST00000646691.1:n.1279C=
ENST00000646777.1:n.1725C=
ENST00000647016.1:n.1872C=
ENST00000647152.1:c.663C=	ENSP00000495893.1:p.Asn221=
ENST00000647209.1:c.*1261C=	ENSP00000495558.1:n.*1261C=
ENST00000647346.1:n.2412C=
ENST00000299427.10:c.1392C=	ENSP00000299427.6:p.Asn464=
ENST00000524611.1:n.270C=
ENST00000533371.5:c.663C=	ENSP00000437066.1:p.Asn221=
ENST00000611494.4:c.1392C=	ENSP00000484546.1:p.Asn464=
NM_000391.3:c.1392C=	NP_000382.3:p.Asn464=
NM_000391.4:c.1392C= MANE Select	NP_000382.3:p.Asn464=