Canonical Allele Identifier: CA1950233860

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615179C= , CM000673.2:g.6615179C=	GRCh38
NC_000011.9:g.6636410C= , CM000673.1:g.6636410C=	GRCh37
NC_000011.8:g.6592986C=	NCBI36
NG_008653.1:g.9283G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1303G=	ENSP00000507321.1:p.Gly435=
ENST00000299427.12:c.1417G= MANE Select	ENSP00000299427.6:p.Gly473=
ENST00000524611.2:n.277G=
ENST00000524924.2:n.537G=
ENST00000533371.6:c.688G=	ENSP00000437066.1:p.Gly230=
ENST00000642892.1:c.688G=	ENSP00000494165.1:p.Gly230=
ENST00000643342.1:c.490G=
ENST00000643439.1:c.*1157G=	ENSP00000495849.1:n.*1157G=
ENST00000643479.1:n.1603G=
ENST00000643516.1:c.926G=
ENST00000644218.1:c.1228G=	ENSP00000493574.1:p.Gly410=
ENST00000644683.1:c.*870G=	ENSP00000494085.1:n.*870G=
ENST00000644810.1:c.1138G=	ENSP00000495895.1:p.Gly380=
ENST00000644831.1:n.1593G=
ENST00000644933.1:c.*283G=	ENSP00000496133.1:n.*283G=
ENST00000645285.1:c.*283G=	ENSP00000495058.1:n.*283G=
ENST00000645331.1:n.2622G=
ENST00000645620.1:c.688G=	ENSP00000493657.1:p.Gly230=
ENST00000646691.1:n.1304G=
ENST00000646777.1:n.1750G=
ENST00000647016.1:n.1897G=
ENST00000647152.1:c.688G=	ENSP00000495893.1:p.Gly230=
ENST00000647209.1:c.*1286G=	ENSP00000495558.1:n.*1286G=
ENST00000647346.1:n.2437G=
ENST00000299427.10:c.1417G=	ENSP00000299427.6:p.Gly473=
ENST00000524611.1:n.295G=
ENST00000533371.5:c.688G=	ENSP00000437066.1:p.Gly230=
ENST00000611494.4:c.1417G=	ENSP00000484546.1:p.Gly473=
NM_000391.3:c.1417G=	NP_000382.3:p.Gly473=
NM_000391.4:c.1417G= MANE Select	NP_000382.3:p.Gly473=