Canonical Allele Identifier: CA1950215312

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617707T= , CM000673.2:g.6617707T=	GRCh38
NC_000011.9:g.6638938T= , CM000673.1:g.6638938T=	GRCh37
NC_000011.8:g.6595514T=	NCBI36
NG_008653.1:g.6755A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.185A=	ENSP00000507321.1:p.Gln62=
ENST00000299427.12:c.299A= MANE Select	ENSP00000299427.6:p.Gln100=
ENST00000428886.7:n.387A=
ENST00000436873.7:c.103A=
ENST00000524788.2:n.1311A=
ENST00000524903.2:n.1427A=
ENST00000528571.6:c.*39A=	ENSP00000434647.1:n.*39A=
ENST00000530040.2:n.328A=
ENST00000533371.6:c.-431A=	ENSP00000437066.1:n.-431A=
ENST00000534644.6:n.300A=
ENST00000642892.1:c.-378A=	ENSP00000494165.1:n.-378A=
ENST00000643439.1:c.*39A=	ENSP00000495849.1:n.*39A=
ENST00000643479.1:n.328A=
ENST00000643516.1:c.186A=
ENST00000644151.1:n.1591A=
ENST00000644218.1:c.299A=	ENSP00000493574.1:p.Gln100=
ENST00000644683.1:c.299A=	ENSP00000494085.1:p.Gln100=
ENST00000644810.1:c.230-554A=	ENSP00000495895.1:n.230-554A=
ENST00000644831.1:n.328A=
ENST00000644933.1:c.-431A=	ENSP00000496133.1:n.-431A=
ENST00000645020.1:n.1327A=
ENST00000645285.1:c.-431A=	ENSP00000495058.1:n.-431A=
ENST00000645331.1:n.321A=
ENST00000645620.1:c.-373A=	ENSP00000493657.1:n.-373A=
ENST00000646777.1:n.328A=
ENST00000647016.1:n.632A=
ENST00000647152.1:c.-431A=	ENSP00000495893.1:n.-431A=
ENST00000647209.1:c.*168A=	ENSP00000495558.1:n.*168A=
ENST00000647346.1:n.1319A=
ENST00000299427.10:c.299A=	ENSP00000299427.6:p.Gln100=
ENST00000428886.6:n.321A=
ENST00000436873.6:c.299A=	ENSP00000398136.2:p.Gln100=
ENST00000528571.5:c.*39A=	ENSP00000434647.1:n.*39A=
ENST00000530040.1:n.411A=
ENST00000533371.5:c.-431A=	ENSP00000437066.1:n.-431A=
ENST00000534644.5:n.284A=
ENST00000611494.4:c.299A=	ENSP00000484546.1:p.Gln100=
NM_000391.3:c.299A=	NP_000382.3:p.Gln100=
NM_000391.4:c.299A= MANE Select	NP_000382.3:p.Gln100=