Canonical Allele Identifier: CA1950237265

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616745G= , CM000673.2:g.6616745G=	GRCh38
NC_000011.9:g.6637976G= , CM000673.1:g.6637976G=	GRCh37
NC_000011.8:g.6594552G=	NCBI36
NG_008653.1:g.7717C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.688C=	ENSP00000507321.1:p.Arg230=
ENST00000299427.12:c.802C= MANE Select	ENSP00000299427.6:p.Arg268=
ENST00000436873.7:c.312+556C=
ENST00000524788.2:n.1961C=
ENST00000524903.2:n.2077C=
ENST00000528807.2:n.458C=
ENST00000530040.2:n.480-242C=
ENST00000533371.6:c.73C=	ENSP00000437066.1:p.Arg25=
ENST00000642892.1:c.73C=	ENSP00000494165.1:p.Arg25=
ENST00000643439.1:c.*542C=	ENSP00000495849.1:n.*542C=
ENST00000643479.1:n.831C=
ENST00000643516.1:c.396-242C=
ENST00000644151.1:n.2241C=
ENST00000644218.1:c.802C=	ENSP00000493574.1:p.Arg268=
ENST00000644683.1:c.*255C=	ENSP00000494085.1:n.*255C=
ENST00000644810.1:c.523C=	ENSP00000495895.1:p.Arg175=
ENST00000644831.1:n.978C=
ENST00000644933.1:c.73C=	ENSP00000496133.1:p.Arg25=
ENST00000645020.1:n.2092C=
ENST00000645285.1:c.73C=	ENSP00000495058.1:p.Arg25=
ENST00000645331.1:n.1168C=
ENST00000645620.1:c.73C=	ENSP00000493657.1:p.Arg25=
ENST00000646777.1:n.978C=
ENST00000647016.1:n.1282C=
ENST00000647152.1:c.73C=	ENSP00000495893.1:p.Arg25=
ENST00000647209.1:c.*671C=	ENSP00000495558.1:n.*671C=
ENST00000647346.1:n.1822C=
ENST00000299427.10:c.802C=	ENSP00000299427.6:p.Arg268=
ENST00000436873.6:c.451-242C=	ENSP00000398136.2:n.451-242C=
ENST00000524788.1:n.502C=
ENST00000528807.1:n.352C=
ENST00000533371.5:c.73C=	ENSP00000437066.1:p.Arg25=
ENST00000611494.4:c.802C=	ENSP00000484546.1:p.Arg268=
NM_000391.3:c.802C=	NP_000382.3:p.Arg268=
NM_000391.4:c.802C= MANE Select	NP_000382.3:p.Arg268=