Canonical Allele Identifier: CA1950234588

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615458G= , CM000673.2:g.6615458G=	GRCh38
NC_000011.9:g.6636689G= , CM000673.1:g.6636689G=	GRCh37
NC_000011.8:g.6593265G=	NCBI36
NG_008653.1:g.9004C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1136C=	ENSP00000507321.1:p.Pro379=
ENST00000299427.12:c.1250C= MANE Select	ENSP00000299427.6:p.Pro417=
ENST00000436873.7:c.487C=
ENST00000524924.2:n.370C=
ENST00000533371.6:c.521C=	ENSP00000437066.1:p.Pro174=
ENST00000642892.1:c.521C=	ENSP00000494165.1:p.Pro174=
ENST00000643342.1:c.323C=
ENST00000643439.1:c.*990C=	ENSP00000495849.1:n.*990C=
ENST00000643479.1:n.1436C=
ENST00000643516.1:c.759C=
ENST00000644218.1:c.1061C=	ENSP00000493574.1:p.Pro354=
ENST00000644683.1:c.*703C=	ENSP00000494085.1:n.*703C=
ENST00000644810.1:c.971C=	ENSP00000495895.1:p.Pro324=
ENST00000644831.1:n.1426C=
ENST00000644933.1:c.*116C=	ENSP00000496133.1:n.*116C=
ENST00000645285.1:c.*116C=	ENSP00000495058.1:n.*116C=
ENST00000645331.1:n.2455C=
ENST00000645620.1:c.521C=	ENSP00000493657.1:p.Pro174=
ENST00000646691.1:n.1025C=
ENST00000646777.1:n.1583C=
ENST00000647016.1:n.1730C=
ENST00000647152.1:c.521C=	ENSP00000495893.1:p.Pro174=
ENST00000647209.1:c.*1119C=	ENSP00000495558.1:n.*1119C=
ENST00000647346.1:n.2270C=
ENST00000299427.10:c.1250C=	ENSP00000299427.6:p.Pro417=
ENST00000524611.1:n.16C=
ENST00000524924.1:n.205C=
ENST00000532191.1:n.303C=
ENST00000533371.5:c.521C=	ENSP00000437066.1:p.Pro174=
ENST00000611494.4:c.1250C=	ENSP00000484546.1:p.Pro417=
NM_000391.3:c.1250C=	NP_000382.3:p.Pro417=
NM_000391.4:c.1250C= MANE Select	NP_000382.3:p.Pro417=