Canonical Allele Identifier: CA1950232766

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614662A= , CM000673.2:g.6614662A=	GRCh38
NC_000011.9:g.6635893A= , CM000673.1:g.6635893A=	GRCh37
NC_000011.8:g.6592469A=	NCBI36
NG_008653.1:g.9800T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1462T=	ENSP00000507321.1:p.Cys488=
ENST00000299427.12:c.1576T= MANE Select	ENSP00000299427.6:p.Cys526=
ENST00000524611.2:n.615T=
ENST00000524924.2:n.696T=
ENST00000533371.6:c.847T=	ENSP00000437066.1:p.Cys283=
ENST00000642892.1:c.847T=	ENSP00000494165.1:p.Cys283=
ENST00000643342.1:c.649T=
ENST00000643439.1:c.*1316T=	ENSP00000495849.1:n.*1316T=
ENST00000643479.1:n.1762T=
ENST00000643516.1:c.1085T=
ENST00000644218.1:c.1387T=	ENSP00000493574.1:p.Cys463=
ENST00000644683.1:c.*1029T=	ENSP00000494085.1:n.*1029T=
ENST00000644810.1:c.1297T=	ENSP00000495895.1:p.Cys433=
ENST00000644831.1:n.1752T=
ENST00000644933.1:c.*442T=	ENSP00000496133.1:n.*442T=
ENST00000645285.1:c.*442T=	ENSP00000495058.1:n.*442T=
ENST00000645331.1:n.2781T=
ENST00000645620.1:c.847T=	ENSP00000493657.1:p.Cys283=
ENST00000646691.1:n.1463T=
ENST00000646777.1:n.1909T=
ENST00000647016.1:n.2056T=
ENST00000647152.1:c.847T=	ENSP00000495893.1:p.Cys283=
ENST00000647209.1:c.*1445T=	ENSP00000495558.1:n.*1445T=
ENST00000647346.1:n.2596T=
ENST00000299427.10:c.1576T=	ENSP00000299427.6:p.Cys526=
ENST00000524611.1:n.454T=
ENST00000533371.5:c.847T=	ENSP00000437066.1:p.Cys283=
ENST00000611494.4:c.1576T=	ENSP00000484546.1:p.Cys526=
NM_000391.3:c.1576T=	NP_000382.3:p.Cys526=
NM_000391.4:c.1576T= MANE Select	NP_000382.3:p.Cys526=