Canonical Allele Identifier: CA1950233972

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615216C= , CM000673.2:g.6615216C=	GRCh38
NC_000011.9:g.6636447C= , CM000673.1:g.6636447C=	GRCh37
NC_000011.8:g.6593023C=	NCBI36
NG_008653.1:g.9246G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1266G=	ENSP00000507321.1:p.Trp422=
ENST00000299427.12:c.1380G= MANE Select	ENSP00000299427.6:p.Trp460=
ENST00000524611.2:n.240G=
ENST00000524924.2:n.500G=
ENST00000533371.6:c.651G=	ENSP00000437066.1:p.Trp217=
ENST00000642892.1:c.651G=	ENSP00000494165.1:p.Trp217=
ENST00000643342.1:c.453G=
ENST00000643439.1:c.*1120G=	ENSP00000495849.1:n.*1120G=
ENST00000643479.1:n.1566G=
ENST00000643516.1:c.889G=
ENST00000644218.1:c.1191G=	ENSP00000493574.1:p.Trp397=
ENST00000644683.1:c.*833G=	ENSP00000494085.1:n.*833G=
ENST00000644810.1:c.1101G=	ENSP00000495895.1:p.Trp367=
ENST00000644831.1:n.1556G=
ENST00000644933.1:c.*246G=	ENSP00000496133.1:n.*246G=
ENST00000645285.1:c.*246G=	ENSP00000495058.1:n.*246G=
ENST00000645331.1:n.2585G=
ENST00000645620.1:c.651G=	ENSP00000493657.1:p.Trp217=
ENST00000646691.1:n.1267G=
ENST00000646777.1:n.1713G=
ENST00000647016.1:n.1860G=
ENST00000647152.1:c.651G=	ENSP00000495893.1:p.Trp217=
ENST00000647209.1:c.*1249G=	ENSP00000495558.1:n.*1249G=
ENST00000647346.1:n.2400G=
ENST00000299427.10:c.1380G=	ENSP00000299427.6:p.Trp460=
ENST00000524611.1:n.258G=
ENST00000532191.1:n.433G=
ENST00000533371.5:c.651G=	ENSP00000437066.1:p.Trp217=
ENST00000611494.4:c.1380G=	ENSP00000484546.1:p.Trp460=
NM_000391.3:c.1380G=	NP_000382.3:p.Trp460=
NM_000391.4:c.1380G= MANE Select	NP_000382.3:p.Trp460=