Canonical Allele Identifier: CA1950232754

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614648C= , CM000673.2:g.6614648C=	GRCh38
NC_000011.9:g.6635879C= , CM000673.1:g.6635879C=	GRCh37
NC_000011.8:g.6592455C=	NCBI36
NG_008653.1:g.9814G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1476G=	ENSP00000507321.1:p.Glu492=
ENST00000299427.12:c.1590G= MANE Select	ENSP00000299427.6:p.Glu530=
ENST00000524611.2:n.629G=
ENST00000524924.2:n.710G=
ENST00000533371.6:c.861G=	ENSP00000437066.1:p.Glu287=
ENST00000642892.1:c.861G=	ENSP00000494165.1:p.Glu287=
ENST00000643342.1:c.663G=
ENST00000643439.1:c.*1330G=	ENSP00000495849.1:n.*1330G=
ENST00000643479.1:n.1776G=
ENST00000643516.1:c.1099G=
ENST00000644218.1:c.1401G=	ENSP00000493574.1:p.Glu467=
ENST00000644683.1:c.*1043G=	ENSP00000494085.1:n.*1043G=
ENST00000644810.1:c.1311G=	ENSP00000495895.1:p.Glu437=
ENST00000644831.1:n.1766G=
ENST00000644933.1:c.*456G=	ENSP00000496133.1:n.*456G=
ENST00000645285.1:c.*456G=	ENSP00000495058.1:n.*456G=
ENST00000645331.1:n.2795G=
ENST00000645620.1:c.861G=	ENSP00000493657.1:p.Glu287=
ENST00000646691.1:n.1477G=
ENST00000646777.1:n.1923G=
ENST00000647016.1:n.2070G=
ENST00000647152.1:c.861G=	ENSP00000495893.1:p.Glu287=
ENST00000647209.1:c.*1459G=	ENSP00000495558.1:n.*1459G=
ENST00000647346.1:n.2610G=
ENST00000299427.10:c.1590G=	ENSP00000299427.6:p.Glu530=
ENST00000524611.1:n.468G=
ENST00000533371.5:c.861G=	ENSP00000437066.1:p.Glu287=
ENST00000611494.4:c.1590G=	ENSP00000484546.1:p.Glu530=
NM_000391.3:c.1590G=	NP_000382.3:p.Glu530=
NM_000391.4:c.1590G= MANE Select	NP_000382.3:p.Glu530=