Canonical Allele Identifier: CA398638312

Gene: TOP3A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18302609T>C , CM000679.2:g.18302609T>C	GRCh38
NC_000017.10:g.18205923T>C , CM000679.1:g.18205923T>C	GRCh37
NC_000017.9:g.18146648T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004618.5:c.614A>G MANE Select	NP_004609.1:p.Asp205Gly
ENST00000321105.10:c.614A>G MANE Select	ENSP00000321636.5:p.Asp205Gly
NM_001320759.1:c.329A>G	NP_001307688.1:p.Asp110Gly
NM_001320759.2:c.329A>G	NP_001307688.1:p.Asp110Gly
NM_004618.3:c.614A>G	NP_004609.1:p.Asp205Gly
NM_004618.4:c.614A>G	NP_004609.1:p.Asp205Gly
ENST00000321105.9:c.614A>G	ENSP00000321636.5:p.Asp205Gly
ENST00000461127.5:c.*232A>G	ENSP00000464338.1:n.*232A>G
ENST00000469739.6:n.493A>G
ENST00000542570.5:c.614A>G	ENSP00000442336.2:p.Asp205Gly
ENST00000580095.5:c.539A>G	ENSP00000462790.1:p.Asp180Gly
ENST00000582981.5:c.*270A>G	ENSP00000462378.1:n.*270A>G
ENST00000583804.2:n.482A>G
ENST00000584582.5:c.*270A>G	ENSP00000462136.1:n.*270A>G
XM_005256776.2:c.329A>G	XP_005256833.1:p.Asp110Gly
XM_011524000.1:c.614A>G	XP_011522302.1:p.Asp205Gly
XM_011524001.1:c.-589A>G	XP_011522303.1:n.-589A>G
XM_011524001.2:c.-589A>G	XP_011522303.1:n.-589A>G
XM_024450903.1:c.-308A>G	XP_024306671.1:n.-308A>G
XR_001752601.2:n.832A>G