Canonical Allele Identifier: CA1950232425

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614473A= , CM000673.2:g.6614473A=	GRCh38
NC_000011.9:g.6635704A= , CM000673.1:g.6635704A=	GRCh37
NC_000011.8:g.6592280A=	NCBI36
NG_008653.1:g.9989T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*73T=	ENSP00000507321.1:n.*73T=
ENST00000299427.12:c.*73T= MANE Select	ENSP00000299427.6:n.*73T=
ENST00000524611.2:n.804T=
ENST00000533371.6:c.*73T=	ENSP00000437066.1:n.*73T=
ENST00000642892.1:c.*73T=	ENSP00000494165.1:n.*73T=
ENST00000643342.1:c.838T=
ENST00000643439.1:c.*1505T=	ENSP00000495849.1:n.*1505T=
ENST00000643479.1:n.1951T=
ENST00000643516.1:c.1274T=
ENST00000644218.1:c.*73T=	ENSP00000493574.1:n.*73T=
ENST00000644683.1:c.*1218T=	ENSP00000494085.1:n.*1218T=
ENST00000644810.1:c.*73T=	ENSP00000495895.1:n.*73T=
ENST00000644831.1:n.1941T=
ENST00000644933.1:c.*631T=	ENSP00000496133.1:n.*631T=
ENST00000645285.1:c.*631T=	ENSP00000495058.1:n.*631T=
ENST00000645331.1:n.2970T=
ENST00000645620.1:c.*73T=	ENSP00000493657.1:n.*73T=
ENST00000646691.1:n.1652T=
ENST00000646777.1:n.2098T=
ENST00000647016.1:n.2245T=
ENST00000647152.1:c.*73T=	ENSP00000495893.1:n.*73T=
ENST00000647209.1:c.*1634T=	ENSP00000495558.1:n.*1634T=
ENST00000647346.1:n.2785T=
ENST00000299427.10:c.*73T=	ENSP00000299427.6:n.*73T=
ENST00000533371.5:c.*73T=	ENSP00000437066.1:n.*73T=
ENST00000611494.4:c.*93T=	ENSP00000484546.1:n.*93T=
NM_000391.3:c.*73T=	NP_000382.3:n.*73T=
NM_000391.4:c.*73T= MANE Select	NP_000382.3:n.*73T=