Canonical Allele Identifier: CA1950233851

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615178C= , CM000673.2:g.6615178C=	GRCh38
NC_000011.9:g.6636409C= , CM000673.1:g.6636409C=	GRCh37
NC_000011.8:g.6592985C=	NCBI36
NG_008653.1:g.9284G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1304G=	ENSP00000507321.1:p.Gly435=
ENST00000299427.12:c.1418G= MANE Select	ENSP00000299427.6:p.Gly473=
ENST00000524611.2:n.278G=
ENST00000524924.2:n.538G=
ENST00000533371.6:c.689G=	ENSP00000437066.1:p.Gly230=
ENST00000642892.1:c.689G=	ENSP00000494165.1:p.Gly230=
ENST00000643342.1:c.491G=
ENST00000643439.1:c.*1158G=	ENSP00000495849.1:n.*1158G=
ENST00000643479.1:n.1604G=
ENST00000643516.1:c.927G=
ENST00000644218.1:c.1229G=	ENSP00000493574.1:p.Gly410=
ENST00000644683.1:c.*871G=	ENSP00000494085.1:n.*871G=
ENST00000644810.1:c.1139G=	ENSP00000495895.1:p.Gly380=
ENST00000644831.1:n.1594G=
ENST00000644933.1:c.*284G=	ENSP00000496133.1:n.*284G=
ENST00000645285.1:c.*284G=	ENSP00000495058.1:n.*284G=
ENST00000645331.1:n.2623G=
ENST00000645620.1:c.689G=	ENSP00000493657.1:p.Gly230=
ENST00000646691.1:n.1305G=
ENST00000646777.1:n.1751G=
ENST00000647016.1:n.1898G=
ENST00000647152.1:c.689G=	ENSP00000495893.1:p.Gly230=
ENST00000647209.1:c.*1287G=	ENSP00000495558.1:n.*1287G=
ENST00000647346.1:n.2438G=
ENST00000299427.10:c.1418G=	ENSP00000299427.6:p.Gly473=
ENST00000524611.1:n.296G=
ENST00000533371.5:c.689G=	ENSP00000437066.1:p.Gly230=
ENST00000611494.4:c.1418G=	ENSP00000484546.1:p.Gly473=
NM_000391.3:c.1418G=	NP_000382.3:p.Gly473=
NM_000391.4:c.1418G= MANE Select	NP_000382.3:p.Gly473=