Canonical Allele Identifier: CA1950234239

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615325T= , CM000673.2:g.6615325T=	GRCh38
NC_000011.9:g.6636556T= , CM000673.1:g.6636556T=	GRCh37
NC_000011.8:g.6593132T=	NCBI36
NG_008653.1:g.9137A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1157A=	ENSP00000507321.1:p.Glu386=
ENST00000299427.12:c.1271A= MANE Select	ENSP00000299427.6:p.Glu424=
ENST00000436873.7:c.508A=
ENST00000524611.2:n.131A=
ENST00000524924.2:n.391A=
ENST00000533371.6:c.542A=	ENSP00000437066.1:p.Glu181=
ENST00000642892.1:c.542A=	ENSP00000494165.1:p.Glu181=
ENST00000643342.1:c.344A=
ENST00000643439.1:c.*1011A=	ENSP00000495849.1:n.*1011A=
ENST00000643479.1:n.1457A=
ENST00000643516.1:c.780A=
ENST00000644218.1:c.1082A=	ENSP00000493574.1:p.Glu361=
ENST00000644683.1:c.*724A=	ENSP00000494085.1:n.*724A=
ENST00000644810.1:c.992A=	ENSP00000495895.1:p.Glu331=
ENST00000644831.1:n.1447A=
ENST00000644933.1:c.*137A=	ENSP00000496133.1:n.*137A=
ENST00000645285.1:c.*137A=	ENSP00000495058.1:n.*137A=
ENST00000645331.1:n.2476A=
ENST00000645620.1:c.542A=	ENSP00000493657.1:p.Glu181=
ENST00000646691.1:n.1158A=
ENST00000646777.1:n.1604A=
ENST00000647016.1:n.1751A=
ENST00000647152.1:c.542A=	ENSP00000495893.1:p.Glu181=
ENST00000647209.1:c.*1140A=	ENSP00000495558.1:n.*1140A=
ENST00000647346.1:n.2291A=
ENST00000299427.10:c.1271A=	ENSP00000299427.6:p.Glu424=
ENST00000524611.1:n.149A=
ENST00000524924.1:n.226A=
ENST00000532191.1:n.324A=
ENST00000533371.5:c.542A=	ENSP00000437066.1:p.Glu181=
ENST00000611494.4:c.1271A=	ENSP00000484546.1:p.Glu424=
NM_000391.3:c.1271A=	NP_000382.3:p.Glu424=
NM_000391.4:c.1271A= MANE Select	NP_000382.3:p.Glu424=