Canonical Allele Identifier: CA1950234216

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615312C= , CM000673.2:g.6615312C=	GRCh38
NC_000011.9:g.6636543C= , CM000673.1:g.6636543C=	GRCh37
NC_000011.8:g.6593119C=	NCBI36
NG_008653.1:g.9150G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1170G=	ENSP00000507321.1:p.Lys390=
ENST00000299427.12:c.1284G= MANE Select	ENSP00000299427.6:p.Lys428=
ENST00000524611.2:n.144G=
ENST00000524924.2:n.404G=
ENST00000533371.6:c.555G=	ENSP00000437066.1:p.Lys185=
ENST00000642892.1:c.555G=	ENSP00000494165.1:p.Lys185=
ENST00000643342.1:c.357G=
ENST00000643439.1:c.*1024G=	ENSP00000495849.1:n.*1024G=
ENST00000643479.1:n.1470G=
ENST00000643516.1:c.793G=
ENST00000644218.1:c.1095G=	ENSP00000493574.1:p.Lys365=
ENST00000644683.1:c.*737G=	ENSP00000494085.1:n.*737G=
ENST00000644810.1:c.1005G=	ENSP00000495895.1:p.Lys335=
ENST00000644831.1:n.1460G=
ENST00000644933.1:c.*150G=	ENSP00000496133.1:n.*150G=
ENST00000645285.1:c.*150G=	ENSP00000495058.1:n.*150G=
ENST00000645331.1:n.2489G=
ENST00000645620.1:c.555G=	ENSP00000493657.1:p.Lys185=
ENST00000646691.1:n.1171G=
ENST00000646777.1:n.1617G=
ENST00000647016.1:n.1764G=
ENST00000647152.1:c.555G=	ENSP00000495893.1:p.Lys185=
ENST00000647209.1:c.*1153G=	ENSP00000495558.1:n.*1153G=
ENST00000647346.1:n.2304G=
ENST00000299427.10:c.1284G=	ENSP00000299427.6:p.Lys428=
ENST00000524611.1:n.162G=
ENST00000524924.1:n.239G=
ENST00000532191.1:n.337G=
ENST00000533371.5:c.555G=	ENSP00000437066.1:p.Lys185=
ENST00000611494.4:c.1284G=	ENSP00000484546.1:p.Lys428=
NM_000391.3:c.1284G=	NP_000382.3:p.Lys428=
NM_000391.4:c.1284G= MANE Select	NP_000382.3:p.Lys428=