Canonical Allele Identifier: CA1950235583

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616026C= , CM000673.2:g.6616026C=	GRCh38
NC_000011.9:g.6637257C= , CM000673.1:g.6637257C=	GRCh37
NC_000011.8:g.6593833C=	NCBI36
NG_008653.1:g.8436G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1010G=	ENSP00000507321.1:p.Arg337=
ENST00000299427.12:c.1124G= MANE Select	ENSP00000299427.6:p.Arg375=
ENST00000436873.7:c.361G=
ENST00000524924.2:n.244G=
ENST00000533371.6:c.395G=	ENSP00000437066.1:p.Arg132=
ENST00000642892.1:c.395G=	ENSP00000494165.1:p.Arg132=
ENST00000643342.1:c.214G=
ENST00000643439.1:c.*864G=	ENSP00000495849.1:n.*864G=
ENST00000643479.1:n.1310G=
ENST00000643516.1:c.633G=
ENST00000644218.1:c.935G=	ENSP00000493574.1:p.Arg312=
ENST00000644683.1:c.*577G=	ENSP00000494085.1:n.*577G=
ENST00000644810.1:c.845G=	ENSP00000495895.1:p.Arg282=
ENST00000644831.1:n.1300G=
ENST00000644933.1:c.395G=	ENSP00000496133.1:p.Arg132=
ENST00000645285.1:c.206G=	ENSP00000495058.1:p.Arg69=
ENST00000645331.1:n.1887G=
ENST00000645620.1:c.395G=	ENSP00000493657.1:p.Arg132=
ENST00000646691.1:n.457G=
ENST00000646777.1:n.1457G=
ENST00000647016.1:n.1604G=
ENST00000647152.1:c.395G=	ENSP00000495893.1:p.Arg132=
ENST00000647209.1:c.*993G=	ENSP00000495558.1:n.*993G=
ENST00000647346.1:n.2144G=
ENST00000299427.10:c.1124G=	ENSP00000299427.6:p.Arg375=
ENST00000524924.1:n.79G=
ENST00000533371.5:c.395G=	ENSP00000437066.1:p.Arg132=
ENST00000611494.4:c.1124G=	ENSP00000484546.1:p.Arg375=
NM_000391.3:c.1124G=	NP_000382.3:p.Arg375=
NM_000391.4:c.1124G= MANE Select	NP_000382.3:p.Arg375=