Canonical Allele Identifier: CA398639833

Gene: TOP3A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321105.10:c.490T>A MANE Select	ENSP00000321636.5:p.Cys164Ser
ENST00000321105.9:c.490T>A	ENSP00000321636.5:p.Cys164Ser
ENST00000461127.5:c.*108T>A	ENSP00000464338.1:n.*108T>A
ENST00000469739.6:n.369T>A
ENST00000542570.5:c.490T>A	ENSP00000442336.2:p.Cys164Ser
ENST00000580095.5:c.415T>A	ENSP00000462790.1:p.Cys139Ser
ENST00000582981.5:c.*146T>A	ENSP00000462378.1:n.*146T>A
ENST00000584582.5:c.*146T>A	ENSP00000462136.1:n.*146T>A
ENST00000584669.5:n.542+1770T>A
NM_004618.3:c.490T>A	NP_004609.1:p.Cys164Ser
XM_005256776.2:c.205T>A	XP_005256833.1:p.Cys69Ser
XM_011524000.1:c.490T>A	XP_011522302.1:p.Cys164Ser
XM_011524001.1:c.-713T>A	XP_011522303.1:n.-713T>A
NM_001320759.1:c.205T>A	NP_001307688.1:p.Cys69Ser
NM_004618.4:c.490T>A	NP_004609.1:p.Cys164Ser
XM_011524001.2:c.-713T>A	XP_011522303.1:n.-713T>A
XM_024450903.1:c.-432T>A	XP_024306671.1:n.-432T>A
XR_001752601.2:n.708T>A
NM_004618.5:c.490T>A MANE Select	NP_004609.1:p.Cys164Ser
NM_001320759.2:c.205T>A	NP_001307688.1:p.Cys69Ser