Canonical Allele Identifier: CA398639808

Gene: TOP3A

Linked Data

• dbSNP Id: rs1466644419
• MyVariant Identifiers: chr17:g.18208431T>C (hg19) ; chr17:g.18305117T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305117T>C , CM000679.2:g.18305117T>C	GRCh38
NC_000017.10:g.18208431T>C , CM000679.1:g.18208431T>C	GRCh37
NC_000017.9:g.18149156T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321105.10:c.494A>G MANE Select	ENSP00000321636.5:p.Lys165Arg
ENST00000321105.9:c.494A>G	ENSP00000321636.5:p.Lys165Arg
ENST00000461127.5:c.*112A>G	ENSP00000464338.1:n.*112A>G
ENST00000469739.6:n.373A>G
ENST00000542570.5:c.494A>G	ENSP00000442336.2:p.Lys165Arg
ENST00000580095.5:c.419A>G	ENSP00000462790.1:p.Lys140Arg
ENST00000582981.5:c.*150A>G	ENSP00000462378.1:n.*150A>G
ENST00000584582.5:c.*150A>G	ENSP00000462136.1:n.*150A>G
ENST00000584669.5:n.542+1774A>G
NM_004618.3:c.494A>G	NP_004609.1:p.Lys165Arg
XM_005256776.2:c.209A>G	XP_005256833.1:p.Lys70Arg
XM_011524000.1:c.494A>G	XP_011522302.1:p.Lys165Arg
XM_011524001.1:c.-709A>G	XP_011522303.1:n.-709A>G
NM_001320759.1:c.209A>G	NP_001307688.1:p.Lys70Arg
NM_004618.4:c.494A>G	NP_004609.1:p.Lys165Arg
XM_011524001.2:c.-709A>G	XP_011522303.1:n.-709A>G
XM_024450903.1:c.-428A>G	XP_024306671.1:n.-428A>G
XR_001752601.2:n.712A>G
NM_004618.5:c.494A>G MANE Select	NP_004609.1:p.Lys165Arg
NM_001320759.2:c.209A>G	NP_001307688.1:p.Lys70Arg