Canonical Allele Identifier: CA1950232476

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614502A= , CM000673.2:g.6614502A=	GRCh38
NC_000011.9:g.6635733A= , CM000673.1:g.6635733A=	GRCh37
NC_000011.8:g.6592309A=	NCBI36
NG_008653.1:g.9960T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*44T=	ENSP00000507321.1:n.*44T=
ENST00000299427.12:c.*44T= MANE Select	ENSP00000299427.6:n.*44T=
ENST00000524611.2:n.775T=
ENST00000533371.6:c.*44T=	ENSP00000437066.1:n.*44T=
ENST00000642892.1:c.*44T=	ENSP00000494165.1:n.*44T=
ENST00000643342.1:c.809T=
ENST00000643439.1:c.*1476T=	ENSP00000495849.1:n.*1476T=
ENST00000643479.1:n.1922T=
ENST00000643516.1:c.1245T=
ENST00000644218.1:c.*44T=	ENSP00000493574.1:n.*44T=
ENST00000644683.1:c.*1189T=	ENSP00000494085.1:n.*1189T=
ENST00000644810.1:c.*44T=	ENSP00000495895.1:n.*44T=
ENST00000644831.1:n.1912T=
ENST00000644933.1:c.*602T=	ENSP00000496133.1:n.*602T=
ENST00000645285.1:c.*602T=	ENSP00000495058.1:n.*602T=
ENST00000645331.1:n.2941T=
ENST00000645620.1:c.*44T=	ENSP00000493657.1:n.*44T=
ENST00000646691.1:n.1623T=
ENST00000646777.1:n.2069T=
ENST00000647016.1:n.2216T=
ENST00000647152.1:c.*44T=	ENSP00000495893.1:n.*44T=
ENST00000647209.1:c.*1605T=	ENSP00000495558.1:n.*1605T=
ENST00000647346.1:n.2756T=
ENST00000299427.10:c.*44T=	ENSP00000299427.6:n.*44T=
ENST00000533371.5:c.*44T=	ENSP00000437066.1:n.*44T=
ENST00000611494.4:c.*64T=	ENSP00000484546.1:n.*64T=
NM_000391.3:c.*44T=	NP_000382.3:n.*44T=
NM_000391.4:c.*44T= MANE Select	NP_000382.3:n.*44T=