Canonical Allele Identifier: CA1950214927

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617378C= , CM000673.2:g.6617378C=	GRCh38
NC_000011.9:g.6638609C= , CM000673.1:g.6638609C=	GRCh37
NC_000011.8:g.6595185C=	NCBI36
NG_008653.1:g.7084G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.317G=	ENSP00000507321.1:p.Gly106=
ENST00000299427.12:c.431G= MANE Select	ENSP00000299427.6:p.Gly144=
ENST00000428886.7:n.519G=
ENST00000436873.7:c.235G=
ENST00000524788.2:n.1443G=
ENST00000524903.2:n.1559G=
ENST00000528571.6:c.*171G=	ENSP00000434647.1:n.*171G=
ENST00000528807.2:n.87G=
ENST00000530040.2:n.460G=
ENST00000533371.6:c.-299G=	ENSP00000437066.1:n.-299G=
ENST00000534644.6:n.432G=
ENST00000642892.1:c.-246G=	ENSP00000494165.1:n.-246G=
ENST00000643439.1:c.*171G=	ENSP00000495849.1:n.*171G=
ENST00000643479.1:n.460G=
ENST00000643516.1:c.318G=
ENST00000644151.1:n.1723G=
ENST00000644218.1:c.431G=	ENSP00000493574.1:p.Gly144=
ENST00000644683.1:c.431G=	ENSP00000494085.1:p.Gly144=
ENST00000644810.1:c.230-225G=	ENSP00000495895.1:n.230-225G=
ENST00000644831.1:n.460G=
ENST00000644933.1:c.-299G=	ENSP00000496133.1:n.-299G=
ENST00000645020.1:n.1459G=
ENST00000645285.1:c.-299G=	ENSP00000495058.1:n.-299G=
ENST00000645331.1:n.650G=
ENST00000645620.1:c.-241G=	ENSP00000493657.1:n.-241G=
ENST00000646777.1:n.460G=
ENST00000647016.1:n.764G=
ENST00000647152.1:c.-299G=	ENSP00000495893.1:n.-299G=
ENST00000647209.1:c.*300G=	ENSP00000495558.1:n.*300G=
ENST00000647346.1:n.1451G=
ENST00000299427.10:c.431G=	ENSP00000299427.6:p.Gly144=
ENST00000428886.6:n.453G=
ENST00000436873.6:c.431G=	ENSP00000398136.2:p.Gly144=
ENST00000528571.5:c.*171G=	ENSP00000434647.1:n.*171G=
ENST00000530040.1:n.543G=
ENST00000533371.5:c.-299G=	ENSP00000437066.1:n.-299G=
ENST00000534644.5:n.416G=
ENST00000611494.4:c.431G=	ENSP00000484546.1:p.Gly144=
NM_000391.3:c.431G=	NP_000382.3:p.Gly144=
NM_000391.4:c.431G= MANE Select	NP_000382.3:p.Gly144=