Canonical Allele Identifier: CA398639796

Gene: TOP3A

Linked Data

• MyVariant Identifiers: chr17:g.18208430C>A (hg19) ; chr17:g.18305116C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305116C>A , CM000679.2:g.18305116C>A	GRCh38
NC_000017.10:g.18208430C>A , CM000679.1:g.18208430C>A	GRCh37
NC_000017.9:g.18149155C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321105.10:c.495G>T MANE Select	ENSP00000321636.5:p.Lys165Asn
ENST00000321105.9:c.495G>T	ENSP00000321636.5:p.Lys165Asn
ENST00000461127.5:c.*113G>T	ENSP00000464338.1:n.*113G>T
ENST00000469739.6:n.374G>T
ENST00000542570.5:c.495G>T	ENSP00000442336.2:p.Lys165Asn
ENST00000580095.5:c.420G>T	ENSP00000462790.1:p.Lys140Asn
ENST00000582981.5:c.*151G>T	ENSP00000462378.1:n.*151G>T
ENST00000584582.5:c.*151G>T	ENSP00000462136.1:n.*151G>T
ENST00000584669.5:n.542+1775G>T
NM_004618.3:c.495G>T	NP_004609.1:p.Lys165Asn
XM_005256776.2:c.210G>T	XP_005256833.1:p.Lys70Asn
XM_011524000.1:c.495G>T	XP_011522302.1:p.Lys165Asn
XM_011524001.1:c.-708G>T	XP_011522303.1:n.-708G>T
NM_001320759.1:c.210G>T	NP_001307688.1:p.Lys70Asn
NM_004618.4:c.495G>T	NP_004609.1:p.Lys165Asn
XM_011524001.2:c.-708G>T	XP_011522303.1:n.-708G>T
XM_024450903.1:c.-427G>T	XP_024306671.1:n.-427G>T
XR_001752601.2:n.713G>T
NM_004618.5:c.495G>T MANE Select	NP_004609.1:p.Lys165Asn
NM_001320759.2:c.210G>T	NP_001307688.1:p.Lys70Asn