Canonical Allele Identifier: CA1950237824

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617034T= , CM000673.2:g.6617034T=	GRCh38
NC_000011.9:g.6638265T= , CM000673.1:g.6638265T=	GRCh37
NC_000011.8:g.6594841T=	NCBI36
NG_008653.1:g.7428A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.514A=	ENSP00000507321.1:p.Asn172=
ENST00000299427.12:c.628A= MANE Select	ENSP00000299427.6:p.Asn210=
ENST00000436873.7:c.312+267A=
ENST00000524788.2:n.1787A=
ENST00000524903.2:n.1903A=
ENST00000528807.2:n.284A=
ENST00000530040.2:n.479+325A=
ENST00000533371.6:c.-102A=	ENSP00000437066.1:n.-102A=
ENST00000534644.6:n.576A=
ENST00000642892.1:c.-102A=	ENSP00000494165.1:n.-102A=
ENST00000643439.1:c.*368A=	ENSP00000495849.1:n.*368A=
ENST00000643479.1:n.657A=
ENST00000643516.1:c.395+267A=
ENST00000644151.1:n.2067A=
ENST00000644218.1:c.628A=	ENSP00000493574.1:p.Asn210=
ENST00000644683.1:c.*81A=	ENSP00000494085.1:n.*81A=
ENST00000644810.1:c.349A=	ENSP00000495895.1:p.Asn117=
ENST00000644831.1:n.804A=
ENST00000644933.1:c.-102A=	ENSP00000496133.1:n.-102A=
ENST00000645020.1:n.1803A=
ENST00000645285.1:c.-102A=	ENSP00000495058.1:n.-102A=
ENST00000645331.1:n.994A=
ENST00000645620.1:c.-102A=	ENSP00000493657.1:n.-102A=
ENST00000646777.1:n.804A=
ENST00000647016.1:n.1108A=
ENST00000647152.1:c.-102A=	ENSP00000495893.1:n.-102A=
ENST00000647209.1:c.*497A=	ENSP00000495558.1:n.*497A=
ENST00000647346.1:n.1648A=
ENST00000299427.10:c.628A=	ENSP00000299427.6:p.Asn210=
ENST00000428886.6:n.797A=
ENST00000436873.6:c.450+325A=	ENSP00000398136.2:n.450+325A=
ENST00000524788.1:n.328A=
ENST00000528571.5:c.*368A=	ENSP00000434647.1:n.*368A=
ENST00000528807.1:n.178A=
ENST00000533371.5:c.-102A=	ENSP00000437066.1:n.-102A=
ENST00000534644.5:n.613A=
ENST00000611494.4:c.628A=	ENSP00000484546.1:p.Asn210=
NM_000391.3:c.628A=	NP_000382.3:p.Asn210=
NM_000391.4:c.628A= MANE Select	NP_000382.3:p.Asn210=