Canonical Allele Identifier: CA1950232676

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614608G= , CM000673.2:g.6614608G=	GRCh38
NC_000011.9:g.6635839G= , CM000673.1:g.6635839G=	GRCh37
NC_000011.8:g.6592415G=	NCBI36
NG_008653.1:g.9854C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1516C=	ENSP00000507321.1:p.Pro506=
ENST00000299427.12:c.1630C= MANE Select	ENSP00000299427.6:p.Pro544=
ENST00000524611.2:n.669C=
ENST00000524924.2:n.750C=
ENST00000533371.6:c.901C=	ENSP00000437066.1:p.Pro301=
ENST00000642892.1:c.901C=	ENSP00000494165.1:p.Pro301=
ENST00000643342.1:c.703C=
ENST00000643439.1:c.*1370C=	ENSP00000495849.1:n.*1370C=
ENST00000643479.1:n.1816C=
ENST00000643516.1:c.1139C=
ENST00000644218.1:c.1441C=	ENSP00000493574.1:p.Pro481=
ENST00000644683.1:c.*1083C=	ENSP00000494085.1:n.*1083C=
ENST00000644810.1:c.1351C=	ENSP00000495895.1:p.Pro451=
ENST00000644831.1:n.1806C=
ENST00000644933.1:c.*496C=	ENSP00000496133.1:n.*496C=
ENST00000645285.1:c.*496C=	ENSP00000495058.1:n.*496C=
ENST00000645331.1:n.2835C=
ENST00000645620.1:c.901C=	ENSP00000493657.1:p.Pro301=
ENST00000646691.1:n.1517C=
ENST00000646777.1:n.1963C=
ENST00000647016.1:n.2110C=
ENST00000647152.1:c.901C=	ENSP00000495893.1:p.Pro301=
ENST00000647209.1:c.*1499C=	ENSP00000495558.1:n.*1499C=
ENST00000647346.1:n.2650C=
ENST00000299427.10:c.1630C=	ENSP00000299427.6:p.Pro544=
ENST00000533371.5:c.901C=	ENSP00000437066.1:p.Pro301=
ENST00000611494.4:c.1630C=	ENSP00000484546.1:p.Pro544=
NM_000391.3:c.1630C=	NP_000382.3:p.Pro544=
NM_000391.4:c.1630C= MANE Select	NP_000382.3:p.Pro544=