Canonical Allele Identifier: CA1950232775

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614668C= , CM000673.2:g.6614668C=	GRCh38
NC_000011.9:g.6635899C= , CM000673.1:g.6635899C=	GRCh37
NC_000011.8:g.6592475C=	NCBI36
NG_008653.1:g.9794G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1456G=	ENSP00000507321.1:p.Glu486=
ENST00000299427.12:c.1570G= MANE Select	ENSP00000299427.6:p.Glu524=
ENST00000524611.2:n.609G=
ENST00000524924.2:n.690G=
ENST00000533371.6:c.841G=	ENSP00000437066.1:p.Glu281=
ENST00000642892.1:c.841G=	ENSP00000494165.1:p.Glu281=
ENST00000643342.1:c.643G=
ENST00000643439.1:c.*1310G=	ENSP00000495849.1:n.*1310G=
ENST00000643479.1:n.1756G=
ENST00000643516.1:c.1079G=
ENST00000644218.1:c.1381G=	ENSP00000493574.1:p.Glu461=
ENST00000644683.1:c.*1023G=	ENSP00000494085.1:n.*1023G=
ENST00000644810.1:c.1291G=	ENSP00000495895.1:p.Glu431=
ENST00000644831.1:n.1746G=
ENST00000644933.1:c.*436G=	ENSP00000496133.1:n.*436G=
ENST00000645285.1:c.*436G=	ENSP00000495058.1:n.*436G=
ENST00000645331.1:n.2775G=
ENST00000645620.1:c.841G=	ENSP00000493657.1:p.Glu281=
ENST00000646691.1:n.1457G=
ENST00000646777.1:n.1903G=
ENST00000647016.1:n.2050G=
ENST00000647152.1:c.841G=	ENSP00000495893.1:p.Glu281=
ENST00000647209.1:c.*1439G=	ENSP00000495558.1:n.*1439G=
ENST00000647346.1:n.2590G=
ENST00000299427.10:c.1570G=	ENSP00000299427.6:p.Glu524=
ENST00000524611.1:n.448G=
ENST00000533371.5:c.841G=	ENSP00000437066.1:p.Glu281=
ENST00000611494.4:c.1570G=	ENSP00000484546.1:p.Glu524=
NM_000391.3:c.1570G=	NP_000382.3:p.Glu524=
NM_000391.4:c.1570G= MANE Select	NP_000382.3:p.Glu524=