Canonical Allele Identifier: CA1950234687

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615503T= , CM000673.2:g.6615503T=	GRCh38
NC_000011.9:g.6636734T= , CM000673.1:g.6636734T=	GRCh37
NC_000011.8:g.6593310T=	NCBI36
NG_008653.1:g.8959A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1091A=	ENSP00000507321.1:p.Glu364=
ENST00000299427.12:c.1205A= MANE Select	ENSP00000299427.6:p.Glu402=
ENST00000436873.7:c.442A=
ENST00000524924.2:n.325A=
ENST00000533371.6:c.476A=	ENSP00000437066.1:p.Glu159=
ENST00000642892.1:c.476A=	ENSP00000494165.1:p.Glu159=
ENST00000643342.1:c.278A=
ENST00000643439.1:c.*945A=	ENSP00000495849.1:n.*945A=
ENST00000643479.1:n.1391A=
ENST00000643516.1:c.714A=
ENST00000644218.1:c.1016A=	ENSP00000493574.1:p.Glu339=
ENST00000644683.1:c.*658A=	ENSP00000494085.1:n.*658A=
ENST00000644810.1:c.926A=	ENSP00000495895.1:p.Glu309=
ENST00000644831.1:n.1381A=
ENST00000644933.1:c.*71A=	ENSP00000496133.1:n.*71A=
ENST00000645285.1:c.*71A=	ENSP00000495058.1:n.*71A=
ENST00000645331.1:n.2410A=
ENST00000645620.1:c.476A=	ENSP00000493657.1:p.Glu159=
ENST00000646691.1:n.980A=
ENST00000646777.1:n.1538A=
ENST00000647016.1:n.1685A=
ENST00000647152.1:c.476A=	ENSP00000495893.1:p.Glu159=
ENST00000647209.1:c.*1074A=	ENSP00000495558.1:n.*1074A=
ENST00000647346.1:n.2225A=
ENST00000299427.10:c.1205A=	ENSP00000299427.6:p.Glu402=
ENST00000524924.1:n.160A=
ENST00000532191.1:n.258A=
ENST00000533371.5:c.476A=	ENSP00000437066.1:p.Glu159=
ENST00000611494.4:c.1205A=	ENSP00000484546.1:p.Glu402=
NM_000391.3:c.1205A=	NP_000382.3:p.Glu402=
NM_000391.4:c.1205A= MANE Select	NP_000382.3:p.Glu402=