Canonical Allele Identifier: CA1950234720

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615527T= , CM000673.2:g.6615527T=	GRCh38
NC_000011.9:g.6636758T= , CM000673.1:g.6636758T=	GRCh37
NC_000011.8:g.6593334T=	NCBI36
NG_008653.1:g.8935A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1067A=	ENSP00000507321.1:p.Gln356=
ENST00000299427.12:c.1181A= MANE Select	ENSP00000299427.6:p.Gln394=
ENST00000436873.7:c.418A=
ENST00000524924.2:n.301A=
ENST00000533371.6:c.452A=	ENSP00000437066.1:p.Gln151=
ENST00000642892.1:c.452A=	ENSP00000494165.1:p.Gln151=
ENST00000643342.1:c.254A=
ENST00000643439.1:c.*921A=	ENSP00000495849.1:n.*921A=
ENST00000643479.1:n.1367A=
ENST00000643516.1:c.690A=
ENST00000644218.1:c.992A=	ENSP00000493574.1:p.Gln331=
ENST00000644683.1:c.*634A=	ENSP00000494085.1:n.*634A=
ENST00000644810.1:c.902A=	ENSP00000495895.1:p.Gln301=
ENST00000644831.1:n.1357A=
ENST00000644933.1:c.*47A=	ENSP00000496133.1:n.*47A=
ENST00000645285.1:c.*47A=	ENSP00000495058.1:n.*47A=
ENST00000645331.1:n.2386A=
ENST00000645620.1:c.452A=	ENSP00000493657.1:p.Gln151=
ENST00000646691.1:n.956A=
ENST00000646777.1:n.1514A=
ENST00000647016.1:n.1661A=
ENST00000647152.1:c.452A=	ENSP00000495893.1:p.Gln151=
ENST00000647209.1:c.*1050A=	ENSP00000495558.1:n.*1050A=
ENST00000647346.1:n.2201A=
ENST00000299427.10:c.1181A=	ENSP00000299427.6:p.Gln394=
ENST00000524924.1:n.136A=
ENST00000532191.1:n.234A=
ENST00000533371.5:c.452A=	ENSP00000437066.1:p.Gln151=
ENST00000611494.4:c.1181A=	ENSP00000484546.1:p.Gln394=
NM_000391.3:c.1181A=	NP_000382.3:p.Gln394=
NM_000391.4:c.1181A= MANE Select	NP_000382.3:p.Gln394=