Canonical Allele Identifier: CA1950214944

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617389G= , CM000673.2:g.6617389G=	GRCh38
NC_000011.9:g.6638620G= , CM000673.1:g.6638620G=	GRCh37
NC_000011.8:g.6595196G=	NCBI36
NG_008653.1:g.7073C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.306C=	ENSP00000507321.1:p.His102=
ENST00000299427.12:c.420C= MANE Select	ENSP00000299427.6:p.His140=
ENST00000428886.7:n.508C=
ENST00000436873.7:c.224C=
ENST00000524788.2:n.1432C=
ENST00000524903.2:n.1548C=
ENST00000528571.6:c.*160C=	ENSP00000434647.1:n.*160C=
ENST00000528807.2:n.76C=
ENST00000530040.2:n.449C=
ENST00000533371.6:c.-310C=	ENSP00000437066.1:n.-310C=
ENST00000534644.6:n.421C=
ENST00000642892.1:c.-257C=	ENSP00000494165.1:n.-257C=
ENST00000643439.1:c.*160C=	ENSP00000495849.1:n.*160C=
ENST00000643479.1:n.449C=
ENST00000643516.1:c.307C=
ENST00000644151.1:n.1712C=
ENST00000644218.1:c.420C=	ENSP00000493574.1:p.His140=
ENST00000644683.1:c.420C=	ENSP00000494085.1:p.His140=
ENST00000644810.1:c.230-236C=	ENSP00000495895.1:n.230-236C=
ENST00000644831.1:n.449C=
ENST00000644933.1:c.-310C=	ENSP00000496133.1:n.-310C=
ENST00000645020.1:n.1448C=
ENST00000645285.1:c.-310C=	ENSP00000495058.1:n.-310C=
ENST00000645331.1:n.639C=
ENST00000645620.1:c.-252C=	ENSP00000493657.1:n.-252C=
ENST00000646777.1:n.449C=
ENST00000647016.1:n.753C=
ENST00000647152.1:c.-310C=	ENSP00000495893.1:n.-310C=
ENST00000647209.1:c.*289C=	ENSP00000495558.1:n.*289C=
ENST00000647346.1:n.1440C=
ENST00000299427.10:c.420C=	ENSP00000299427.6:p.His140=
ENST00000428886.6:n.442C=
ENST00000436873.6:c.420C=	ENSP00000398136.2:p.His140=
ENST00000528571.5:c.*160C=	ENSP00000434647.1:n.*160C=
ENST00000530040.1:n.532C=
ENST00000533371.5:c.-310C=	ENSP00000437066.1:n.-310C=
ENST00000534644.5:n.405C=
ENST00000611494.4:c.420C=	ENSP00000484546.1:p.His140=
NM_000391.3:c.420C=	NP_000382.3:p.His140=
NM_000391.4:c.420C= MANE Select	NP_000382.3:p.His140=