Canonical Allele Identifier: CA1950234057

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615245C= , CM000673.2:g.6615245C=	GRCh38
NC_000011.9:g.6636476C= , CM000673.1:g.6636476C=	GRCh37
NC_000011.8:g.6593052C=	NCBI36
NG_008653.1:g.9217G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1237G=	ENSP00000507321.1:p.Asp413=
ENST00000299427.12:c.1351G= MANE Select	ENSP00000299427.6:p.Asp451=
ENST00000524611.2:n.211G=
ENST00000524924.2:n.471G=
ENST00000533371.6:c.622G=	ENSP00000437066.1:p.Asp208=
ENST00000642892.1:c.622G=	ENSP00000494165.1:p.Asp208=
ENST00000643342.1:c.424G=
ENST00000643439.1:c.*1091G=	ENSP00000495849.1:n.*1091G=
ENST00000643479.1:n.1537G=
ENST00000643516.1:c.860G=
ENST00000644218.1:c.1162G=	ENSP00000493574.1:p.Asp388=
ENST00000644683.1:c.*804G=	ENSP00000494085.1:n.*804G=
ENST00000644810.1:c.1072G=	ENSP00000495895.1:p.Asp358=
ENST00000644831.1:n.1527G=
ENST00000644933.1:c.*217G=	ENSP00000496133.1:n.*217G=
ENST00000645285.1:c.*217G=	ENSP00000495058.1:n.*217G=
ENST00000645331.1:n.2556G=
ENST00000645620.1:c.622G=	ENSP00000493657.1:p.Asp208=
ENST00000646691.1:n.1238G=
ENST00000646777.1:n.1684G=
ENST00000647016.1:n.1831G=
ENST00000647152.1:c.622G=	ENSP00000495893.1:p.Asp208=
ENST00000647209.1:c.*1220G=	ENSP00000495558.1:n.*1220G=
ENST00000647346.1:n.2371G=
ENST00000299427.10:c.1351G=	ENSP00000299427.6:p.Asp451=
ENST00000524611.1:n.229G=
ENST00000532191.1:n.404G=
ENST00000533371.5:c.622G=	ENSP00000437066.1:p.Asp208=
ENST00000611494.4:c.1351G=	ENSP00000484546.1:p.Asp451=
NM_000391.3:c.1351G=	NP_000382.3:p.Asp451=
NM_000391.4:c.1351G= MANE Select	NP_000382.3:p.Asp451=