Canonical Allele Identifier: CA398639818

Gene: TOP3A

Linked Data

• MyVariant Identifiers: chr17:g.18208432T>C (hg19) ; chr17:g.18305118T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305118T>C , CM000679.2:g.18305118T>C	GRCh38
NC_000017.10:g.18208432T>C , CM000679.1:g.18208432T>C	GRCh37
NC_000017.9:g.18149157T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321105.10:c.493A>G MANE Select	ENSP00000321636.5:p.Lys165Glu
ENST00000321105.9:c.493A>G	ENSP00000321636.5:p.Lys165Glu
ENST00000461127.5:c.*111A>G	ENSP00000464338.1:n.*111A>G
ENST00000469739.6:n.372A>G
ENST00000542570.5:c.493A>G	ENSP00000442336.2:p.Lys165Glu
ENST00000580095.5:c.418A>G	ENSP00000462790.1:p.Lys140Glu
ENST00000582981.5:c.*149A>G	ENSP00000462378.1:n.*149A>G
ENST00000584582.5:c.*149A>G	ENSP00000462136.1:n.*149A>G
ENST00000584669.5:n.542+1773A>G
NM_004618.3:c.493A>G	NP_004609.1:p.Lys165Glu
XM_005256776.2:c.208A>G	XP_005256833.1:p.Lys70Glu
XM_011524000.1:c.493A>G	XP_011522302.1:p.Lys165Glu
XM_011524001.1:c.-710A>G	XP_011522303.1:n.-710A>G
NM_001320759.1:c.208A>G	NP_001307688.1:p.Lys70Glu
NM_004618.4:c.493A>G	NP_004609.1:p.Lys165Glu
XM_011524001.2:c.-710A>G	XP_011522303.1:n.-710A>G
XM_024450903.1:c.-429A>G	XP_024306671.1:n.-429A>G
XR_001752601.2:n.711A>G
NM_004618.5:c.493A>G MANE Select	NP_004609.1:p.Lys165Glu
NM_001320759.2:c.208A>G	NP_001307688.1:p.Lys70Glu