Canonical Allele Identifier: CA1950234037

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615234T= , CM000673.2:g.6615234T=	GRCh38
NC_000011.9:g.6636465T= , CM000673.1:g.6636465T=	GRCh37
NC_000011.8:g.6593041T=	NCBI36
NG_008653.1:g.9228A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1248A=	ENSP00000507321.1:p.Ala416=
ENST00000299427.12:c.1362A= MANE Select	ENSP00000299427.6:p.Ala454=
ENST00000524611.2:n.222A=
ENST00000524924.2:n.482A=
ENST00000533371.6:c.633A=	ENSP00000437066.1:p.Ala211=
ENST00000642892.1:c.633A=	ENSP00000494165.1:p.Ala211=
ENST00000643342.1:c.435A=
ENST00000643439.1:c.*1102A=	ENSP00000495849.1:n.*1102A=
ENST00000643479.1:n.1548A=
ENST00000643516.1:c.871A=
ENST00000644218.1:c.1173A=	ENSP00000493574.1:p.Ala391=
ENST00000644683.1:c.*815A=	ENSP00000494085.1:n.*815A=
ENST00000644810.1:c.1083A=	ENSP00000495895.1:p.Ala361=
ENST00000644831.1:n.1538A=
ENST00000644933.1:c.*228A=	ENSP00000496133.1:n.*228A=
ENST00000645285.1:c.*228A=	ENSP00000495058.1:n.*228A=
ENST00000645331.1:n.2567A=
ENST00000645620.1:c.633A=	ENSP00000493657.1:p.Ala211=
ENST00000646691.1:n.1249A=
ENST00000646777.1:n.1695A=
ENST00000647016.1:n.1842A=
ENST00000647152.1:c.633A=	ENSP00000495893.1:p.Ala211=
ENST00000647209.1:c.*1231A=	ENSP00000495558.1:n.*1231A=
ENST00000647346.1:n.2382A=
ENST00000299427.10:c.1362A=	ENSP00000299427.6:p.Ala454=
ENST00000524611.1:n.240A=
ENST00000532191.1:n.415A=
ENST00000533371.5:c.633A=	ENSP00000437066.1:p.Ala211=
ENST00000611494.4:c.1362A=	ENSP00000484546.1:p.Ala454=
NM_000391.3:c.1362A=	NP_000382.3:p.Ala454=
NM_000391.4:c.1362A= MANE Select	NP_000382.3:p.Ala454=