Canonical Allele Identifier: CA1950214933

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617382C= , CM000673.2:g.6617382C=	GRCh38
NC_000011.9:g.6638613C= , CM000673.1:g.6638613C=	GRCh37
NC_000011.8:g.6595189C=	NCBI36
NG_008653.1:g.7080G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.313G=	ENSP00000507321.1:p.Gly105=
ENST00000299427.12:c.427G= MANE Select	ENSP00000299427.6:p.Gly143=
ENST00000428886.7:n.515G=
ENST00000436873.7:c.231G=
ENST00000524788.2:n.1439G=
ENST00000524903.2:n.1555G=
ENST00000528571.6:c.*167G=	ENSP00000434647.1:n.*167G=
ENST00000528807.2:n.83G=
ENST00000530040.2:n.456G=
ENST00000533371.6:c.-303G=	ENSP00000437066.1:n.-303G=
ENST00000534644.6:n.428G=
ENST00000642892.1:c.-250G=	ENSP00000494165.1:n.-250G=
ENST00000643439.1:c.*167G=	ENSP00000495849.1:n.*167G=
ENST00000643479.1:n.456G=
ENST00000643516.1:c.314G=
ENST00000644151.1:n.1719G=
ENST00000644218.1:c.427G=	ENSP00000493574.1:p.Gly143=
ENST00000644683.1:c.427G=	ENSP00000494085.1:p.Gly143=
ENST00000644810.1:c.230-229G=	ENSP00000495895.1:n.230-229G=
ENST00000644831.1:n.456G=
ENST00000644933.1:c.-303G=	ENSP00000496133.1:n.-303G=
ENST00000645020.1:n.1455G=
ENST00000645285.1:c.-303G=	ENSP00000495058.1:n.-303G=
ENST00000645331.1:n.646G=
ENST00000645620.1:c.-245G=	ENSP00000493657.1:n.-245G=
ENST00000646777.1:n.456G=
ENST00000647016.1:n.760G=
ENST00000647152.1:c.-303G=	ENSP00000495893.1:n.-303G=
ENST00000647209.1:c.*296G=	ENSP00000495558.1:n.*296G=
ENST00000647346.1:n.1447G=
ENST00000299427.10:c.427G=	ENSP00000299427.6:p.Gly143=
ENST00000428886.6:n.449G=
ENST00000436873.6:c.427G=	ENSP00000398136.2:p.Gly143=
ENST00000528571.5:c.*167G=	ENSP00000434647.1:n.*167G=
ENST00000530040.1:n.539G=
ENST00000533371.5:c.-303G=	ENSP00000437066.1:n.-303G=
ENST00000534644.5:n.412G=
ENST00000611494.4:c.427G=	ENSP00000484546.1:p.Gly143=
NM_000391.3:c.427G=	NP_000382.3:p.Gly143=
NM_000391.4:c.427G= MANE Select	NP_000382.3:p.Gly143=