Canonical Allele Identifier: CA1950234717

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615526C= , CM000673.2:g.6615526C=	GRCh38
NC_000011.9:g.6636757C= , CM000673.1:g.6636757C=	GRCh37
NC_000011.8:g.6593333C=	NCBI36
NG_008653.1:g.8936G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1068G=	ENSP00000507321.1:p.Gln356=
ENST00000299427.12:c.1182G= MANE Select	ENSP00000299427.6:p.Gln394=
ENST00000436873.7:c.419G=
ENST00000524924.2:n.302G=
ENST00000533371.6:c.453G=	ENSP00000437066.1:p.Gln151=
ENST00000642892.1:c.453G=	ENSP00000494165.1:p.Gln151=
ENST00000643342.1:c.255G=
ENST00000643439.1:c.*922G=	ENSP00000495849.1:n.*922G=
ENST00000643479.1:n.1368G=
ENST00000643516.1:c.691G=
ENST00000644218.1:c.993G=	ENSP00000493574.1:p.Gln331=
ENST00000644683.1:c.*635G=	ENSP00000494085.1:n.*635G=
ENST00000644810.1:c.903G=	ENSP00000495895.1:p.Gln301=
ENST00000644831.1:n.1358G=
ENST00000644933.1:c.*48G=	ENSP00000496133.1:n.*48G=
ENST00000645285.1:c.*48G=	ENSP00000495058.1:n.*48G=
ENST00000645331.1:n.2387G=
ENST00000645620.1:c.453G=	ENSP00000493657.1:p.Gln151=
ENST00000646691.1:n.957G=
ENST00000646777.1:n.1515G=
ENST00000647016.1:n.1662G=
ENST00000647152.1:c.453G=	ENSP00000495893.1:p.Gln151=
ENST00000647209.1:c.*1051G=	ENSP00000495558.1:n.*1051G=
ENST00000647346.1:n.2202G=
ENST00000299427.10:c.1182G=	ENSP00000299427.6:p.Gln394=
ENST00000524924.1:n.137G=
ENST00000532191.1:n.235G=
ENST00000533371.5:c.453G=	ENSP00000437066.1:p.Gln151=
ENST00000611494.4:c.1182G=	ENSP00000484546.1:p.Gln394=
NM_000391.3:c.1182G=	NP_000382.3:p.Gln394=
NM_000391.4:c.1182G= MANE Select	NP_000382.3:p.Gln394=