Canonical Allele Identifier: CA398639813

Gene: TOP3A

Linked Data

• MyVariant Identifiers: chr17:g.18208431T>G (hg19) ; chr17:g.18305117T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000321105.10:c.494A>C MANE Select	ENSP00000321636.5:p.Lys165Thr
ENST00000321105.9:c.494A>C	ENSP00000321636.5:p.Lys165Thr
ENST00000461127.5:c.*112A>C	ENSP00000464338.1:n.*112A>C
ENST00000469739.6:n.373A>C
ENST00000542570.5:c.494A>C	ENSP00000442336.2:p.Lys165Thr
ENST00000580095.5:c.419A>C	ENSP00000462790.1:p.Lys140Thr
ENST00000582981.5:c.*150A>C	ENSP00000462378.1:n.*150A>C
ENST00000584582.5:c.*150A>C	ENSP00000462136.1:n.*150A>C
ENST00000584669.5:n.542+1774A>C
NM_004618.3:c.494A>C	NP_004609.1:p.Lys165Thr
XM_005256776.2:c.209A>C	XP_005256833.1:p.Lys70Thr
XM_011524000.1:c.494A>C	XP_011522302.1:p.Lys165Thr
XM_011524001.1:c.-709A>C	XP_011522303.1:n.-709A>C
NM_001320759.1:c.209A>C	NP_001307688.1:p.Lys70Thr
NM_004618.4:c.494A>C	NP_004609.1:p.Lys165Thr
XM_011524001.2:c.-709A>C	XP_011522303.1:n.-709A>C
XM_024450903.1:c.-428A>C	XP_024306671.1:n.-428A>C
XR_001752601.2:n.712A>C
NM_004618.5:c.494A>C MANE Select	NP_004609.1:p.Lys165Thr
NM_001320759.2:c.209A>C	NP_001307688.1:p.Lys70Thr