Canonical Allele Identifier: CA1950232655

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614600T= , CM000673.2:g.6614600T=	GRCh38
NC_000011.9:g.6635831T= , CM000673.1:g.6635831T=	GRCh37
NC_000011.8:g.6592407T=	NCBI36
NG_008653.1:g.9862A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.1524A=	ENSP00000507321.1:p.Thr508=
ENST00000299427.12:c.1638A= MANE Select	ENSP00000299427.6:p.Thr546=
ENST00000524611.2:n.677A=
ENST00000533371.6:c.909A=	ENSP00000437066.1:p.Thr303=
ENST00000642892.1:c.909A=	ENSP00000494165.1:p.Thr303=
ENST00000643342.1:c.711A=
ENST00000643439.1:c.*1378A=	ENSP00000495849.1:n.*1378A=
ENST00000643479.1:n.1824A=
ENST00000643516.1:c.1147A=
ENST00000644218.1:c.1449A=	ENSP00000493574.1:p.Thr483=
ENST00000644683.1:c.*1091A=	ENSP00000494085.1:n.*1091A=
ENST00000644810.1:c.1359A=	ENSP00000495895.1:p.Thr453=
ENST00000644831.1:n.1814A=
ENST00000644933.1:c.*504A=	ENSP00000496133.1:n.*504A=
ENST00000645285.1:c.*504A=	ENSP00000495058.1:n.*504A=
ENST00000645331.1:n.2843A=
ENST00000645620.1:c.909A=	ENSP00000493657.1:p.Thr303=
ENST00000646691.1:n.1525A=
ENST00000646777.1:n.1971A=
ENST00000647016.1:n.2118A=
ENST00000647152.1:c.909A=	ENSP00000495893.1:p.Thr303=
ENST00000647209.1:c.*1507A=	ENSP00000495558.1:n.*1507A=
ENST00000647346.1:n.2658A=
ENST00000299427.10:c.1638A=	ENSP00000299427.6:p.Thr546=
ENST00000533371.5:c.909A=	ENSP00000437066.1:p.Thr303=
ENST00000611494.4:c.1638A=	ENSP00000484546.1:p.Thr546=
NM_000391.3:c.1638A=	NP_000382.3:p.Thr546=
NM_000391.4:c.1638A= MANE Select	NP_000382.3:p.Thr546=