Canonical Allele Identifier: CA1950232773

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614667T= , CM000673.2:g.6614667T=	GRCh38
NC_000011.9:g.6635898T= , CM000673.1:g.6635898T=	GRCh37
NC_000011.8:g.6592474T=	NCBI36
NG_008653.1:g.9795A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1457A=	ENSP00000507321.1:p.Glu486=
ENST00000299427.12:c.1571A= MANE Select	ENSP00000299427.6:p.Glu524=
ENST00000524611.2:n.610A=
ENST00000524924.2:n.691A=
ENST00000533371.6:c.842A=	ENSP00000437066.1:p.Glu281=
ENST00000642892.1:c.842A=	ENSP00000494165.1:p.Glu281=
ENST00000643342.1:c.644A=
ENST00000643439.1:c.*1311A=	ENSP00000495849.1:n.*1311A=
ENST00000643479.1:n.1757A=
ENST00000643516.1:c.1080A=
ENST00000644218.1:c.1382A=	ENSP00000493574.1:p.Glu461=
ENST00000644683.1:c.*1024A=	ENSP00000494085.1:n.*1024A=
ENST00000644810.1:c.1292A=	ENSP00000495895.1:p.Glu431=
ENST00000644831.1:n.1747A=
ENST00000644933.1:c.*437A=	ENSP00000496133.1:n.*437A=
ENST00000645285.1:c.*437A=	ENSP00000495058.1:n.*437A=
ENST00000645331.1:n.2776A=
ENST00000645620.1:c.842A=	ENSP00000493657.1:p.Glu281=
ENST00000646691.1:n.1458A=
ENST00000646777.1:n.1904A=
ENST00000647016.1:n.2051A=
ENST00000647152.1:c.842A=	ENSP00000495893.1:p.Glu281=
ENST00000647209.1:c.*1440A=	ENSP00000495558.1:n.*1440A=
ENST00000647346.1:n.2591A=
ENST00000299427.10:c.1571A=	ENSP00000299427.6:p.Glu524=
ENST00000524611.1:n.449A=
ENST00000533371.5:c.842A=	ENSP00000437066.1:p.Glu281=
ENST00000611494.4:c.1571A=	ENSP00000484546.1:p.Glu524=
NM_000391.3:c.1571A=	NP_000382.3:p.Glu524=
NM_000391.4:c.1571A= MANE Select	NP_000382.3:p.Glu524=