Canonical Allele Identifier: CA1950237340

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616779T= , CM000673.2:g.6616779T=	GRCh38
NC_000011.9:g.6638010T= , CM000673.1:g.6638010T=	GRCh37
NC_000011.8:g.6594586T=	NCBI36
NG_008653.1:g.7683A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.654A=	ENSP00000507321.1:p.Ser218=
ENST00000299427.12:c.768A= MANE Select	ENSP00000299427.6:p.Ser256=
ENST00000436873.7:c.312+522A=
ENST00000524788.2:n.1927A=
ENST00000524903.2:n.2043A=
ENST00000528807.2:n.424A=
ENST00000530040.2:n.480-276A=
ENST00000533371.6:c.39A=	ENSP00000437066.1:p.Ser13=
ENST00000642892.1:c.39A=	ENSP00000494165.1:p.Ser13=
ENST00000643439.1:c.*508A=	ENSP00000495849.1:n.*508A=
ENST00000643479.1:n.797A=
ENST00000643516.1:c.396-276A=
ENST00000644151.1:n.2207A=
ENST00000644218.1:c.768A=	ENSP00000493574.1:p.Ser256=
ENST00000644683.1:c.*221A=	ENSP00000494085.1:n.*221A=
ENST00000644810.1:c.489A=	ENSP00000495895.1:p.Ser163=
ENST00000644831.1:n.944A=
ENST00000644933.1:c.39A=	ENSP00000496133.1:p.Ser13=
ENST00000645020.1:n.2058A=
ENST00000645285.1:c.39A=	ENSP00000495058.1:p.Ser13=
ENST00000645331.1:n.1134A=
ENST00000645620.1:c.39A=	ENSP00000493657.1:p.Ser13=
ENST00000646777.1:n.944A=
ENST00000647016.1:n.1248A=
ENST00000647152.1:c.39A=	ENSP00000495893.1:p.Ser13=
ENST00000647209.1:c.*637A=	ENSP00000495558.1:n.*637A=
ENST00000647346.1:n.1788A=
ENST00000299427.10:c.768A=	ENSP00000299427.6:p.Ser256=
ENST00000436873.6:c.451-276A=	ENSP00000398136.2:n.451-276A=
ENST00000524788.1:n.468A=
ENST00000528807.1:n.318A=
ENST00000533371.5:c.39A=	ENSP00000437066.1:p.Ser13=
ENST00000611494.4:c.768A=	ENSP00000484546.1:p.Ser256=
NM_000391.3:c.768A=	NP_000382.3:p.Ser256=
NM_000391.4:c.768A= MANE Select	NP_000382.3:p.Ser256=