Canonical Allele Identifier: CA8429619

Gene: TOP3A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18278185T>C , CM000679.2:g.18278185T>C	GRCh38
NC_000017.10:g.18181499T>C , CM000679.1:g.18181499T>C	GRCh37
NC_000017.9:g.18122224T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004618.5:c.2317A>G MANE Select	NP_004609.1:p.Asn773Asp
ENST00000321105.10:c.2317A>G MANE Select	ENSP00000321636.5:p.Asn773Asp
NM_001320759.1:c.2032A>G	NP_001307688.1:p.Asn678Asp
NM_001320759.2:c.2032A>G	NP_001307688.1:p.Asn678Asp
NM_004618.3:c.2317A>G	NP_004609.1:p.Asn773Asp
NM_004618.4:c.2317A>G	NP_004609.1:p.Asn773Asp
ENST00000321105.9:c.2317A>G	ENSP00000321636.5:p.Asn773Asp
ENST00000469739.6:n.1672A>G
ENST00000542570.5:c.2317A>G	ENSP00000442336.2:p.Asn773Asp
ENST00000580095.5:c.2242A>G	ENSP00000462790.1:p.Asn748Asp
ENST00000582981.5:c.*1973A>G	ENSP00000462378.1:n.*1973A>G
ENST00000584582.5:c.*1973A>G	ENSP00000462136.1:n.*1973A>G
XM_005256776.2:c.2032A>G	XP_005256833.1:p.Asn678Asp
XM_011524001.1:c.907A>G	XP_011522303.1:p.Asn303Asp
XM_011524001.2:c.907A>G	XP_011522303.1:p.Asn303Asp
XM_024450903.1:c.1396A>G	XP_024306671.1:p.Asn466Asp
XR_001752601.2:n.2592A>G