Canonical Allele Identifier: CA1950233926

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615203T= , CM000673.2:g.6615203T=	GRCh38
NC_000011.9:g.6636434T= , CM000673.1:g.6636434T=	GRCh37
NC_000011.8:g.6593010T=	NCBI36
NG_008653.1:g.9259A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1279A=	ENSP00000507321.1:p.Arg427=
ENST00000299427.12:c.1393A= MANE Select	ENSP00000299427.6:p.Arg465=
ENST00000524611.2:n.253A=
ENST00000524924.2:n.513A=
ENST00000533371.6:c.664A=	ENSP00000437066.1:p.Arg222=
ENST00000642892.1:c.664A=	ENSP00000494165.1:p.Arg222=
ENST00000643342.1:c.466A=
ENST00000643439.1:c.*1133A=	ENSP00000495849.1:n.*1133A=
ENST00000643479.1:n.1579A=
ENST00000643516.1:c.902A=
ENST00000644218.1:c.1204A=	ENSP00000493574.1:p.Arg402=
ENST00000644683.1:c.*846A=	ENSP00000494085.1:n.*846A=
ENST00000644810.1:c.1114A=	ENSP00000495895.1:p.Arg372=
ENST00000644831.1:n.1569A=
ENST00000644933.1:c.*259A=	ENSP00000496133.1:n.*259A=
ENST00000645285.1:c.*259A=	ENSP00000495058.1:n.*259A=
ENST00000645331.1:n.2598A=
ENST00000645620.1:c.664A=	ENSP00000493657.1:p.Arg222=
ENST00000646691.1:n.1280A=
ENST00000646777.1:n.1726A=
ENST00000647016.1:n.1873A=
ENST00000647152.1:c.664A=	ENSP00000495893.1:p.Arg222=
ENST00000647209.1:c.*1262A=	ENSP00000495558.1:n.*1262A=
ENST00000647346.1:n.2413A=
ENST00000299427.10:c.1393A=	ENSP00000299427.6:p.Arg465=
ENST00000524611.1:n.271A=
ENST00000533371.5:c.664A=	ENSP00000437066.1:p.Arg222=
ENST00000611494.4:c.1393A=	ENSP00000484546.1:p.Arg465=
NM_000391.3:c.1393A=	NP_000382.3:p.Arg465=
NM_000391.4:c.1393A= MANE Select	NP_000382.3:p.Arg465=