Canonical Allele Identifier: CA398639831

Gene: TOP3A

Linked Data

• MyVariant Identifiers: chr17:g.18208435A>G (hg19) ; chr17:g.18305121A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305121A>G , CM000679.2:g.18305121A>G	GRCh38
NC_000017.10:g.18208435A>G , CM000679.1:g.18208435A>G	GRCh37
NC_000017.9:g.18149160A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321105.10:c.490T>C MANE Select	ENSP00000321636.5:p.Cys164Arg
ENST00000321105.9:c.490T>C	ENSP00000321636.5:p.Cys164Arg
ENST00000461127.5:c.*108T>C	ENSP00000464338.1:n.*108T>C
ENST00000469739.6:n.369T>C
ENST00000542570.5:c.490T>C	ENSP00000442336.2:p.Cys164Arg
ENST00000580095.5:c.415T>C	ENSP00000462790.1:p.Cys139Arg
ENST00000582981.5:c.*146T>C	ENSP00000462378.1:n.*146T>C
ENST00000584582.5:c.*146T>C	ENSP00000462136.1:n.*146T>C
ENST00000584669.5:n.542+1770T>C
NM_004618.3:c.490T>C	NP_004609.1:p.Cys164Arg
XM_005256776.2:c.205T>C	XP_005256833.1:p.Cys69Arg
XM_011524000.1:c.490T>C	XP_011522302.1:p.Cys164Arg
XM_011524001.1:c.-713T>C	XP_011522303.1:n.-713T>C
NM_001320759.1:c.205T>C	NP_001307688.1:p.Cys69Arg
NM_004618.4:c.490T>C	NP_004609.1:p.Cys164Arg
XM_011524001.2:c.-713T>C	XP_011522303.1:n.-713T>C
XM_024450903.1:c.-432T>C	XP_024306671.1:n.-432T>C
XR_001752601.2:n.708T>C
NM_004618.5:c.490T>C MANE Select	NP_004609.1:p.Cys164Arg
NM_001320759.2:c.205T>C	NP_001307688.1:p.Cys69Arg