Canonical Allele Identifier: CA1950232492

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614508A= , CM000673.2:g.6614508A=	GRCh38
NC_000011.9:g.6635739A= , CM000673.1:g.6635739A=	GRCh37
NC_000011.8:g.6592315A=	NCBI36
NG_008653.1:g.9954T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*38T=	ENSP00000507321.1:n.*38T=
ENST00000299427.12:c.*38T= MANE Select	ENSP00000299427.6:n.*38T=
ENST00000524611.2:n.769T=
ENST00000533371.6:c.*38T=	ENSP00000437066.1:n.*38T=
ENST00000642892.1:c.*38T=	ENSP00000494165.1:n.*38T=
ENST00000643342.1:c.803T=
ENST00000643439.1:c.*1470T=	ENSP00000495849.1:n.*1470T=
ENST00000643479.1:n.1916T=
ENST00000643516.1:c.1239T=
ENST00000644218.1:c.*38T=	ENSP00000493574.1:n.*38T=
ENST00000644683.1:c.*1183T=	ENSP00000494085.1:n.*1183T=
ENST00000644810.1:c.*38T=	ENSP00000495895.1:n.*38T=
ENST00000644831.1:n.1906T=
ENST00000644933.1:c.*596T=	ENSP00000496133.1:n.*596T=
ENST00000645285.1:c.*596T=	ENSP00000495058.1:n.*596T=
ENST00000645331.1:n.2935T=
ENST00000645620.1:c.*38T=	ENSP00000493657.1:n.*38T=
ENST00000646691.1:n.1617T=
ENST00000646777.1:n.2063T=
ENST00000647016.1:n.2210T=
ENST00000647152.1:c.*38T=	ENSP00000495893.1:n.*38T=
ENST00000647209.1:c.*1599T=	ENSP00000495558.1:n.*1599T=
ENST00000647346.1:n.2750T=
ENST00000299427.10:c.*38T=	ENSP00000299427.6:n.*38T=
ENST00000533371.5:c.*38T=	ENSP00000437066.1:n.*38T=
ENST00000611494.4:c.*58T=	ENSP00000484546.1:n.*58T=
NM_000391.3:c.*38T=	NP_000382.3:n.*38T=
NM_000391.4:c.*38T= MANE Select	NP_000382.3:n.*38T=