Canonical Allele Identifier: CA1950215243

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617656T= , CM000673.2:g.6617656T=	GRCh38
NC_000011.9:g.6638887T= , CM000673.1:g.6638887T=	GRCh37
NC_000011.8:g.6595463T=	NCBI36
NG_008653.1:g.6806A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.236A=	ENSP00000507321.1:p.Gln79=
ENST00000299427.12:c.350A= MANE Select	ENSP00000299427.6:p.Gln117=
ENST00000428886.7:n.438A=
ENST00000436873.7:c.154A=
ENST00000524788.2:n.1362A=
ENST00000524903.2:n.1478A=
ENST00000528571.6:c.*90A=	ENSP00000434647.1:n.*90A=
ENST00000530040.2:n.379A=
ENST00000533371.6:c.-380A=	ENSP00000437066.1:n.-380A=
ENST00000534644.6:n.351A=
ENST00000642892.1:c.-327A=	ENSP00000494165.1:n.-327A=
ENST00000643439.1:c.*90A=	ENSP00000495849.1:n.*90A=
ENST00000643479.1:n.379A=
ENST00000643516.1:c.237A=
ENST00000644151.1:n.1642A=
ENST00000644218.1:c.350A=	ENSP00000493574.1:p.Gln117=
ENST00000644683.1:c.350A=	ENSP00000494085.1:p.Gln117=
ENST00000644810.1:c.230-503A=	ENSP00000495895.1:n.230-503A=
ENST00000644831.1:n.379A=
ENST00000644933.1:c.-380A=	ENSP00000496133.1:n.-380A=
ENST00000645020.1:n.1378A=
ENST00000645285.1:c.-380A=	ENSP00000495058.1:n.-380A=
ENST00000645331.1:n.372A=
ENST00000645620.1:c.-322A=	ENSP00000493657.1:n.-322A=
ENST00000646777.1:n.379A=
ENST00000647016.1:n.683A=
ENST00000647152.1:c.-380A=	ENSP00000495893.1:n.-380A=
ENST00000647209.1:c.*219A=	ENSP00000495558.1:n.*219A=
ENST00000647346.1:n.1370A=
ENST00000299427.10:c.350A=	ENSP00000299427.6:p.Gln117=
ENST00000428886.6:n.372A=
ENST00000436873.6:c.350A=	ENSP00000398136.2:p.Gln117=
ENST00000528571.5:c.*90A=	ENSP00000434647.1:n.*90A=
ENST00000530040.1:n.462A=
ENST00000533371.5:c.-380A=	ENSP00000437066.1:n.-380A=
ENST00000534644.5:n.335A=
ENST00000611494.4:c.350A=	ENSP00000484546.1:p.Gln117=
NM_000391.3:c.350A=	NP_000382.3:p.Gln117=
NM_000391.4:c.350A= MANE Select	NP_000382.3:p.Gln117=