Canonical Allele Identifier: CA510555035

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744947T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116307T>C , CM000682.2:g.41116307T>C	GRCh38
NC_000020.10:g.39744947T>C , CM000682.1:g.39744947T>C	GRCh37
NC_000020.9:g.39178361T>C	NCBI36
NG_012262.1:g.92486T>C
NG_012262.2:g.92486T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1737T>C (TOP1) MANE Select	ENSP00000354522.2:p.Asp579=
ENST00000680945.1:c.330T>C (TOP1)	ENSP00000504935.1:p.Asp110=
ENST00000681058.1:n.6523T>C (TOP1)
ENST00000681113.1:c.*1432T>C (TOP1)	ENSP00000505788.1:n.*1432T>C
ENST00000681392.1:n.3045T>C (TOP1)
ENST00000681884.1:n.2999T>C (TOP1)
ENST00000361337.2:c.1737T>C (TOP1)	ENSP00000354522.2:p.Asp579=
NM_003286.2:c.1737T>C (TOP1)	NP_003277.1:p.Asp579=
NR_109889.1:n.711-15018A>G (PLCG1-AS1)
XM_011529032.1:c.1233T>C (TOP1)	XP_011527334.1:p.Asp411=
XM_011529033.1:c.999T>C (TOP1)	XP_011527335.1:p.Asp333=
NM_003286.3:c.1737T>C (TOP1)	NP_003277.1:p.Asp579=
NM_003286.4:c.1737T>C (TOP1) MANE Select	NP_003277.1:p.Asp579=