Canonical Allele Identifier: CA1950232435

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614476A= , CM000673.2:g.6614476A=	GRCh38
NC_000011.9:g.6635707A= , CM000673.1:g.6635707A=	GRCh37
NC_000011.8:g.6592283A=	NCBI36
NG_008653.1:g.9986T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*70T=	ENSP00000507321.1:n.*70T=
ENST00000299427.12:c.*70T= MANE Select	ENSP00000299427.6:n.*70T=
ENST00000524611.2:n.801T=
ENST00000533371.6:c.*70T=	ENSP00000437066.1:n.*70T=
ENST00000642892.1:c.*70T=	ENSP00000494165.1:n.*70T=
ENST00000643342.1:c.835T=
ENST00000643439.1:c.*1502T=	ENSP00000495849.1:n.*1502T=
ENST00000643479.1:n.1948T=
ENST00000643516.1:c.1271T=
ENST00000644218.1:c.*70T=	ENSP00000493574.1:n.*70T=
ENST00000644683.1:c.*1215T=	ENSP00000494085.1:n.*1215T=
ENST00000644810.1:c.*70T=	ENSP00000495895.1:n.*70T=
ENST00000644831.1:n.1938T=
ENST00000644933.1:c.*628T=	ENSP00000496133.1:n.*628T=
ENST00000645285.1:c.*628T=	ENSP00000495058.1:n.*628T=
ENST00000645331.1:n.2967T=
ENST00000645620.1:c.*70T=	ENSP00000493657.1:n.*70T=
ENST00000646691.1:n.1649T=
ENST00000646777.1:n.2095T=
ENST00000647016.1:n.2242T=
ENST00000647152.1:c.*70T=	ENSP00000495893.1:n.*70T=
ENST00000647209.1:c.*1631T=	ENSP00000495558.1:n.*1631T=
ENST00000647346.1:n.2782T=
ENST00000299427.10:c.*70T=	ENSP00000299427.6:n.*70T=
ENST00000533371.5:c.*70T=	ENSP00000437066.1:n.*70T=
ENST00000611494.4:c.*90T=	ENSP00000484546.1:n.*90T=
NM_000391.3:c.*70T=	NP_000382.3:n.*70T=
NM_000391.4:c.*70T= MANE Select	NP_000382.3:n.*70T=