Canonical Allele Identifier: CA1950232503

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614523C= , CM000673.2:g.6614523C=	GRCh38
NC_000011.9:g.6635754C= , CM000673.1:g.6635754C=	GRCh37
NC_000011.8:g.6592330C=	NCBI36
NG_008653.1:g.9939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*23G=	ENSP00000507321.1:n.*23G=
ENST00000299427.12:c.*23G= MANE Select	ENSP00000299427.6:n.*23G=
ENST00000524611.2:n.754G=
ENST00000533371.6:c.*23G=	ENSP00000437066.1:n.*23G=
ENST00000642892.1:c.*23G=	ENSP00000494165.1:n.*23G=
ENST00000643342.1:c.788G=
ENST00000643439.1:c.*1455G=	ENSP00000495849.1:n.*1455G=
ENST00000643479.1:n.1901G=
ENST00000643516.1:c.1224G=
ENST00000644218.1:c.*23G=	ENSP00000493574.1:n.*23G=
ENST00000644683.1:c.*1168G=	ENSP00000494085.1:n.*1168G=
ENST00000644810.1:c.*23G=	ENSP00000495895.1:n.*23G=
ENST00000644831.1:n.1891G=
ENST00000644933.1:c.*581G=	ENSP00000496133.1:n.*581G=
ENST00000645285.1:c.*581G=	ENSP00000495058.1:n.*581G=
ENST00000645331.1:n.2920G=
ENST00000645620.1:c.*23G=	ENSP00000493657.1:n.*23G=
ENST00000646691.1:n.1602G=
ENST00000646777.1:n.2048G=
ENST00000647016.1:n.2195G=
ENST00000647152.1:c.*23G=	ENSP00000495893.1:n.*23G=
ENST00000647209.1:c.*1584G=	ENSP00000495558.1:n.*1584G=
ENST00000647346.1:n.2735G=
ENST00000299427.10:c.*23G=	ENSP00000299427.6:n.*23G=
ENST00000533371.5:c.*23G=	ENSP00000437066.1:n.*23G=
ENST00000611494.4:c.*43G=	ENSP00000484546.1:n.*43G=
NM_000391.3:c.*23G=	NP_000382.3:n.*23G=
NM_000391.4:c.*23G= MANE Select	NP_000382.3:n.*23G=