Canonical Allele Identifier: CA1950234768

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615548G= , CM000673.2:g.6615548G=	GRCh38
NC_000011.9:g.6636779G= , CM000673.1:g.6636779G=	GRCh37
NC_000011.8:g.6593355G=	NCBI36
NG_008653.1:g.8914C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1046C=	ENSP00000507321.1:p.Thr349=
ENST00000299427.12:c.1160C= MANE Select	ENSP00000299427.6:p.Thr387=
ENST00000436873.7:c.397C=
ENST00000524924.2:n.280C=
ENST00000533371.6:c.431C=	ENSP00000437066.1:p.Thr144=
ENST00000642892.1:c.431C=	ENSP00000494165.1:p.Thr144=
ENST00000643342.1:c.236-3C=
ENST00000643439.1:c.*900C=	ENSP00000495849.1:n.*900C=
ENST00000643479.1:n.1346C=
ENST00000643516.1:c.669C=
ENST00000644218.1:c.971C=	ENSP00000493574.1:p.Thr324=
ENST00000644683.1:c.*613C=	ENSP00000494085.1:n.*613C=
ENST00000644810.1:c.881C=	ENSP00000495895.1:p.Thr294=
ENST00000644831.1:n.1336C=
ENST00000644933.1:c.*26C=	ENSP00000496133.1:n.*26C=
ENST00000645285.1:c.*26C=	ENSP00000495058.1:n.*26C=
ENST00000645331.1:n.2365C=
ENST00000645620.1:c.431C=	ENSP00000493657.1:p.Thr144=
ENST00000646691.1:n.935C=
ENST00000646777.1:n.1493C=
ENST00000647016.1:n.1640C=
ENST00000647152.1:c.431C=	ENSP00000495893.1:p.Thr144=
ENST00000647209.1:c.*1029C=	ENSP00000495558.1:n.*1029C=
ENST00000647346.1:n.2180C=
ENST00000299427.10:c.1160C=	ENSP00000299427.6:p.Thr387=
ENST00000524924.1:n.115C=
ENST00000532191.1:n.213C=
ENST00000533371.5:c.431C=	ENSP00000437066.1:p.Thr144=
ENST00000611494.4:c.1160C=	ENSP00000484546.1:p.Thr387=
NM_000391.3:c.1160C=	NP_000382.3:p.Thr387=
NM_000391.4:c.1160C= MANE Select	NP_000382.3:p.Thr387=