Canonical Allele Identifier: CA1950237333

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616775C= , CM000673.2:g.6616775C=	GRCh38
NC_000011.9:g.6638006C= , CM000673.1:g.6638006C=	GRCh37
NC_000011.8:g.6594582C=	NCBI36
NG_008653.1:g.7687G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.658G=	ENSP00000507321.1:p.Ala220=
ENST00000299427.12:c.772G= MANE Select	ENSP00000299427.6:p.Ala258=
ENST00000436873.7:c.312+526G=
ENST00000524788.2:n.1931G=
ENST00000524903.2:n.2047G=
ENST00000528807.2:n.428G=
ENST00000530040.2:n.480-272G=
ENST00000533371.6:c.43G=	ENSP00000437066.1:p.Ala15=
ENST00000642892.1:c.43G=	ENSP00000494165.1:p.Ala15=
ENST00000643439.1:c.*512G=	ENSP00000495849.1:n.*512G=
ENST00000643479.1:n.801G=
ENST00000643516.1:c.396-272G=
ENST00000644151.1:n.2211G=
ENST00000644218.1:c.772G=	ENSP00000493574.1:p.Ala258=
ENST00000644683.1:c.*225G=	ENSP00000494085.1:n.*225G=
ENST00000644810.1:c.493G=	ENSP00000495895.1:p.Ala165=
ENST00000644831.1:n.948G=
ENST00000644933.1:c.43G=	ENSP00000496133.1:p.Ala15=
ENST00000645020.1:n.2062G=
ENST00000645285.1:c.43G=	ENSP00000495058.1:p.Ala15=
ENST00000645331.1:n.1138G=
ENST00000645620.1:c.43G=	ENSP00000493657.1:p.Ala15=
ENST00000646777.1:n.948G=
ENST00000647016.1:n.1252G=
ENST00000647152.1:c.43G=	ENSP00000495893.1:p.Ala15=
ENST00000647209.1:c.*641G=	ENSP00000495558.1:n.*641G=
ENST00000647346.1:n.1792G=
ENST00000299427.10:c.772G=	ENSP00000299427.6:p.Ala258=
ENST00000436873.6:c.451-272G=	ENSP00000398136.2:n.451-272G=
ENST00000524788.1:n.472G=
ENST00000528807.1:n.322G=
ENST00000533371.5:c.43G=	ENSP00000437066.1:p.Ala15=
ENST00000611494.4:c.772G=	ENSP00000484546.1:p.Ala258=
NM_000391.3:c.772G=	NP_000382.3:p.Ala258=
NM_000391.4:c.772G= MANE Select	NP_000382.3:p.Ala258=