Canonical Allele Identifier: CA2250934326

Gene: TOP3A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305111C= , CM000679.2:g.18305111C=	GRCh38
NC_000017.10:g.18208425C= , CM000679.1:g.18208425C=	GRCh37
NC_000017.9:g.18149150C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321105.10:c.499+1G= MANE Select	ENSP00000321636.5:n.499+1G=
ENST00000321105.9:c.499+1G=	ENSP00000321636.5:n.499+1G=
ENST00000461127.5:c.*117+1G=	ENSP00000464338.1:n.*117+1G=
ENST00000469739.6:n.378+1G=
ENST00000542570.5:c.499+1G=	ENSP00000442336.2:n.499+1G=
ENST00000580095.5:c.424+1G=	ENSP00000462790.1:n.424+1G=
ENST00000582981.5:c.*155+1G=	ENSP00000462378.1:n.*155+1G=
ENST00000584582.5:c.*155+1G=	ENSP00000462136.1:n.*155+1G=
ENST00000584669.5:n.542+1780G=
NM_004618.3:c.499+1G=	NP_004609.1:n.499+1G=
XM_005256776.2:c.214+1G=	XP_005256833.1:n.214+1G=
XM_011524000.1:c.499+1G=	XP_011522302.1:n.499+1G=
XM_011524001.1:c.-704+1G=	XP_011522303.1:n.-704+1G=
NM_001320759.1:c.214+1G=	NP_001307688.1:n.214+1G=
NM_004618.4:c.499+1G=	NP_004609.1:n.499+1G=
XM_011524001.2:c.-704+1G=	XP_011522303.1:n.-704+1G=
XM_024450903.1:c.-423+1G=	XP_024306671.1:n.-423+1G=
XR_001752601.2:n.717+1G=
NM_004618.5:c.499+1G= MANE Select	NP_004609.1:n.499+1G=
NM_001320759.2:c.214+1G=	NP_001307688.1:n.214+1G=