Canonical Allele Identifier: CA1950235557

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616019G= , CM000673.2:g.6616019G=	GRCh38
NC_000011.9:g.6637250G= , CM000673.1:g.6637250G=	GRCh37
NC_000011.8:g.6593826G=	NCBI36
NG_008653.1:g.8443C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1017C=	ENSP00000507321.1:p.Thr339=
ENST00000299427.12:c.1131C= MANE Select	ENSP00000299427.6:p.Thr377=
ENST00000436873.7:c.368C=
ENST00000524924.2:n.251C=
ENST00000533371.6:c.402C=	ENSP00000437066.1:p.Thr134=
ENST00000642892.1:c.402C=	ENSP00000494165.1:p.Thr134=
ENST00000643342.1:c.221C=
ENST00000643439.1:c.*871C=	ENSP00000495849.1:n.*871C=
ENST00000643479.1:n.1317C=
ENST00000643516.1:c.640C=
ENST00000644218.1:c.942C=	ENSP00000493574.1:p.Thr314=
ENST00000644683.1:c.*584C=	ENSP00000494085.1:n.*584C=
ENST00000644810.1:c.852C=	ENSP00000495895.1:p.Thr284=
ENST00000644831.1:n.1307C=
ENST00000644933.1:c.402C=	ENSP00000496133.1:p.Thr134=
ENST00000645285.1:c.213C=	ENSP00000495058.1:p.Thr71=
ENST00000645331.1:n.1894C=
ENST00000645620.1:c.402C=	ENSP00000493657.1:p.Thr134=
ENST00000646691.1:n.464C=
ENST00000646777.1:n.1464C=
ENST00000647016.1:n.1611C=
ENST00000647152.1:c.402C=	ENSP00000495893.1:p.Thr134=
ENST00000647209.1:c.*1000C=	ENSP00000495558.1:n.*1000C=
ENST00000647346.1:n.2151C=
ENST00000299427.10:c.1131C=	ENSP00000299427.6:p.Thr377=
ENST00000524924.1:n.86C=
ENST00000533371.5:c.402C=	ENSP00000437066.1:p.Thr134=
ENST00000611494.4:c.1131C=	ENSP00000484546.1:p.Thr377=
NM_000391.3:c.1131C=	NP_000382.3:p.Thr377=
NM_000391.4:c.1131C= MANE Select	NP_000382.3:p.Thr377=