Canonical Allele Identifier: CA1950215217

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617626C= , CM000673.2:g.6617626C=	GRCh38
NC_000011.9:g.6638857C= , CM000673.1:g.6638857C=	GRCh37
NC_000011.8:g.6595433C=	NCBI36
NG_008653.1:g.6836G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.266G=	ENSP00000507321.1:p.Arg89=
ENST00000299427.12:c.380G= MANE Select	ENSP00000299427.6:p.Arg127=
ENST00000428886.7:n.468G=
ENST00000436873.7:c.184G=
ENST00000524788.2:n.1392G=
ENST00000524903.2:n.1508G=
ENST00000528571.6:c.*120G=	ENSP00000434647.1:n.*120G=
ENST00000530040.2:n.409G=
ENST00000533371.6:c.-350G=	ENSP00000437066.1:n.-350G=
ENST00000534644.6:n.381G=
ENST00000642892.1:c.-297G=	ENSP00000494165.1:n.-297G=
ENST00000643439.1:c.*120G=	ENSP00000495849.1:n.*120G=
ENST00000643479.1:n.409G=
ENST00000643516.1:c.267G=
ENST00000644151.1:n.1672G=
ENST00000644218.1:c.380G=	ENSP00000493574.1:p.Arg127=
ENST00000644683.1:c.380G=	ENSP00000494085.1:p.Arg127=
ENST00000644810.1:c.230-473G=	ENSP00000495895.1:n.230-473G=
ENST00000644831.1:n.409G=
ENST00000644933.1:c.-350G=	ENSP00000496133.1:n.-350G=
ENST00000645020.1:n.1408G=
ENST00000645285.1:c.-350G=	ENSP00000495058.1:n.-350G=
ENST00000645331.1:n.402G=
ENST00000645620.1:c.-292G=	ENSP00000493657.1:n.-292G=
ENST00000646777.1:n.409G=
ENST00000647016.1:n.713G=
ENST00000647152.1:c.-350G=	ENSP00000495893.1:n.-350G=
ENST00000647209.1:c.*249G=	ENSP00000495558.1:n.*249G=
ENST00000647346.1:n.1400G=
ENST00000299427.10:c.380G=	ENSP00000299427.6:p.Arg127=
ENST00000428886.6:n.402G=
ENST00000436873.6:c.380G=	ENSP00000398136.2:p.Arg127=
ENST00000528571.5:c.*120G=	ENSP00000434647.1:n.*120G=
ENST00000530040.1:n.492G=
ENST00000533371.5:c.-350G=	ENSP00000437066.1:n.-350G=
ENST00000534644.5:n.365G=
ENST00000611494.4:c.380G=	ENSP00000484546.1:p.Arg127=
NM_000391.3:c.380G=	NP_000382.3:p.Arg127=
NM_000391.4:c.380G= MANE Select	NP_000382.3:p.Arg127=