Canonical Allele Identifier: CA1950232644

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614594C= , CM000673.2:g.6614594C=	GRCh38
NC_000011.9:g.6635825C= , CM000673.1:g.6635825C=	GRCh37
NC_000011.8:g.6592401C=	NCBI36
NG_008653.1:g.9868G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.1530G=	ENSP00000507321.1:p.Trp510=
ENST00000299427.12:c.1644G= MANE Select	ENSP00000299427.6:p.Trp548=
ENST00000524611.2:n.683G=
ENST00000533371.6:c.915G=	ENSP00000437066.1:p.Trp305=
ENST00000642892.1:c.915G=	ENSP00000494165.1:p.Trp305=
ENST00000643342.1:c.717G=
ENST00000643439.1:c.*1384G=	ENSP00000495849.1:n.*1384G=
ENST00000643479.1:n.1830G=
ENST00000643516.1:c.1153G=
ENST00000644218.1:c.1455G=	ENSP00000493574.1:p.Trp485=
ENST00000644683.1:c.*1097G=	ENSP00000494085.1:n.*1097G=
ENST00000644810.1:c.1365G=	ENSP00000495895.1:p.Trp455=
ENST00000644831.1:n.1820G=
ENST00000644933.1:c.*510G=	ENSP00000496133.1:n.*510G=
ENST00000645285.1:c.*510G=	ENSP00000495058.1:n.*510G=
ENST00000645331.1:n.2849G=
ENST00000645620.1:c.915G=	ENSP00000493657.1:p.Trp305=
ENST00000646691.1:n.1531G=
ENST00000646777.1:n.1977G=
ENST00000647016.1:n.2124G=
ENST00000647152.1:c.915G=	ENSP00000495893.1:p.Trp305=
ENST00000647209.1:c.*1513G=	ENSP00000495558.1:n.*1513G=
ENST00000647346.1:n.2664G=
ENST00000299427.10:c.1644G=	ENSP00000299427.6:p.Trp548=
ENST00000533371.5:c.915G=	ENSP00000437066.1:p.Trp305=
ENST00000611494.4:c.1644G=	ENSP00000484546.1:p.Trp548=
NM_000391.3:c.1644G=	NP_000382.3:p.Trp548=
NM_000391.4:c.1644G= MANE Select	NP_000382.3:p.Trp548=