Canonical Allele Identifier: CA1950237119

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616669C= , CM000673.2:g.6616669C=	GRCh38
NC_000011.9:g.6637900C= , CM000673.1:g.6637900C=	GRCh37
NC_000011.8:g.6594476C=	NCBI36
NG_008653.1:g.7793G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.764G=	ENSP00000507321.1:p.Ser255=
ENST00000299427.12:c.878G= MANE Select	ENSP00000299427.6:p.Ser293=
ENST00000436873.7:c.313-595G=
ENST00000524788.2:n.2037G=
ENST00000524903.2:n.2153G=
ENST00000528807.2:n.534G=
ENST00000530040.2:n.480-166G=
ENST00000533371.6:c.149G=	ENSP00000437066.1:p.Ser50=
ENST00000642892.1:c.149G=	ENSP00000494165.1:p.Ser50=
ENST00000643439.1:c.*618G=	ENSP00000495849.1:n.*618G=
ENST00000643479.1:n.907G=
ENST00000643516.1:c.396-166G=
ENST00000644151.1:n.2317G=
ENST00000644218.1:c.878G=	ENSP00000493574.1:p.Ser293=
ENST00000644683.1:c.*331G=	ENSP00000494085.1:n.*331G=
ENST00000644810.1:c.599G=	ENSP00000495895.1:p.Ser200=
ENST00000644831.1:n.1054G=
ENST00000644933.1:c.149G=	ENSP00000496133.1:p.Ser50=
ENST00000645020.1:n.2168G=
ENST00000645285.1:c.149G=	ENSP00000495058.1:p.Ser50=
ENST00000645331.1:n.1244G=
ENST00000645620.1:c.149G=	ENSP00000493657.1:p.Ser50=
ENST00000646777.1:n.1054G=
ENST00000647016.1:n.1358G=
ENST00000647152.1:c.149G=	ENSP00000495893.1:p.Ser50=
ENST00000647209.1:c.*747G=	ENSP00000495558.1:n.*747G=
ENST00000647346.1:n.1898G=
ENST00000299427.10:c.878G=	ENSP00000299427.6:p.Ser293=
ENST00000436873.6:c.451-166G=	ENSP00000398136.2:n.451-166G=
ENST00000528807.1:n.428G=
ENST00000533371.5:c.149G=	ENSP00000437066.1:p.Ser50=
ENST00000611494.4:c.878G=	ENSP00000484546.1:p.Ser293=
NM_000391.3:c.878G=	NP_000382.3:p.Ser293=
NM_000391.4:c.878G= MANE Select	NP_000382.3:p.Ser293=