Canonical Allele Identifier: CA1950237108

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616666C= , CM000673.2:g.6616666C=	GRCh38
NC_000011.9:g.6637897C= , CM000673.1:g.6637897C=	GRCh37
NC_000011.8:g.6594473C=	NCBI36
NG_008653.1:g.7796G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.767G=	ENSP00000507321.1:p.Ser256=
ENST00000299427.12:c.881G= MANE Select	ENSP00000299427.6:p.Ser294=
ENST00000436873.7:c.313-592G=
ENST00000524788.2:n.2040G=
ENST00000524903.2:n.2156G=
ENST00000528807.2:n.537G=
ENST00000530040.2:n.480-163G=
ENST00000533371.6:c.152G=	ENSP00000437066.1:p.Ser51=
ENST00000642892.1:c.152G=	ENSP00000494165.1:p.Ser51=
ENST00000643439.1:c.*621G=	ENSP00000495849.1:n.*621G=
ENST00000643479.1:n.910G=
ENST00000643516.1:c.396-163G=
ENST00000644151.1:n.2320G=
ENST00000644218.1:c.881G=	ENSP00000493574.1:p.Ser294=
ENST00000644683.1:c.*334G=	ENSP00000494085.1:n.*334G=
ENST00000644810.1:c.602G=	ENSP00000495895.1:p.Ser201=
ENST00000644831.1:n.1057G=
ENST00000644933.1:c.152G=	ENSP00000496133.1:p.Ser51=
ENST00000645020.1:n.2171G=
ENST00000645285.1:c.152G=	ENSP00000495058.1:p.Ser51=
ENST00000645331.1:n.1247G=
ENST00000645620.1:c.152G=	ENSP00000493657.1:p.Ser51=
ENST00000646777.1:n.1057G=
ENST00000647016.1:n.1361G=
ENST00000647152.1:c.152G=	ENSP00000495893.1:p.Ser51=
ENST00000647209.1:c.*750G=	ENSP00000495558.1:n.*750G=
ENST00000647346.1:n.1901G=
ENST00000299427.10:c.881G=	ENSP00000299427.6:p.Ser294=
ENST00000436873.6:c.451-163G=	ENSP00000398136.2:n.451-163G=
ENST00000528807.1:n.431G=
ENST00000533371.5:c.152G=	ENSP00000437066.1:p.Ser51=
ENST00000611494.4:c.881G=	ENSP00000484546.1:p.Ser294=
NM_000391.3:c.881G=	NP_000382.3:p.Ser294=
NM_000391.4:c.881G= MANE Select	NP_000382.3:p.Ser294=