Canonical Allele Identifier: CA1950234742

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615538G= , CM000673.2:g.6615538G=	GRCh38
NC_000011.9:g.6636769G= , CM000673.1:g.6636769G=	GRCh37
NC_000011.8:g.6593345G=	NCBI36
NG_008653.1:g.8924C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1056C=	ENSP00000507321.1:p.Gly352=
ENST00000299427.12:c.1170C= MANE Select	ENSP00000299427.6:p.Gly390=
ENST00000436873.7:c.407C=
ENST00000524924.2:n.290C=
ENST00000533371.6:c.441C=	ENSP00000437066.1:p.Gly147=
ENST00000642892.1:c.441C=	ENSP00000494165.1:p.Gly147=
ENST00000643342.1:c.243C=
ENST00000643439.1:c.*910C=	ENSP00000495849.1:n.*910C=
ENST00000643479.1:n.1356C=
ENST00000643516.1:c.679C=
ENST00000644218.1:c.981C=	ENSP00000493574.1:p.Gly327=
ENST00000644683.1:c.*623C=	ENSP00000494085.1:n.*623C=
ENST00000644810.1:c.891C=	ENSP00000495895.1:p.Gly297=
ENST00000644831.1:n.1346C=
ENST00000644933.1:c.*36C=	ENSP00000496133.1:n.*36C=
ENST00000645285.1:c.*36C=	ENSP00000495058.1:n.*36C=
ENST00000645331.1:n.2375C=
ENST00000645620.1:c.441C=	ENSP00000493657.1:p.Gly147=
ENST00000646691.1:n.945C=
ENST00000646777.1:n.1503C=
ENST00000647016.1:n.1650C=
ENST00000647152.1:c.441C=	ENSP00000495893.1:p.Gly147=
ENST00000647209.1:c.*1039C=	ENSP00000495558.1:n.*1039C=
ENST00000647346.1:n.2190C=
ENST00000299427.10:c.1170C=	ENSP00000299427.6:p.Gly390=
ENST00000524924.1:n.125C=
ENST00000532191.1:n.223C=
ENST00000533371.5:c.441C=	ENSP00000437066.1:p.Gly147=
ENST00000611494.4:c.1170C=	ENSP00000484546.1:p.Gly390=
NM_000391.3:c.1170C=	NP_000382.3:p.Gly390=
NM_000391.4:c.1170C= MANE Select	NP_000382.3:p.Gly390=