Canonical Allele Identifier: CA409021854

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744978C>A (hg19) ; chr20:g.41116338C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116338C>A , CM000682.2:g.41116338C>A	GRCh38
NC_000020.10:g.39744978C>A , CM000682.1:g.39744978C>A	GRCh37
NC_000020.9:g.39178392C>A	NCBI36
NG_012262.1:g.92517C>A
NG_012262.2:g.92517C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361337.3:c.1768C>A (TOP1) MANE Select	ENSP00000354522.2:p.Arg590Ser
ENST00000680945.1:c.361C>A (TOP1)	ENSP00000504935.1:p.Arg121Ser
ENST00000681058.1:n.6554C>A (TOP1)
ENST00000681113.1:c.*1463C>A (TOP1)	ENSP00000505788.1:n.*1463C>A
ENST00000681392.1:n.3076C>A (TOP1)
ENST00000681884.1:n.3030C>A (TOP1)
ENST00000361337.2:c.1768C>A (TOP1)	ENSP00000354522.2:p.Arg590Ser
NM_003286.2:c.1768C>A (TOP1)	NP_003277.1:p.Arg590Ser
NR_109889.1:n.711-15049G>T (PLCG1-AS1)
XM_011529032.1:c.1264C>A (TOP1)	XP_011527334.1:p.Arg422Ser
XM_011529033.1:c.1030C>A (TOP1)	XP_011527335.1:p.Arg344Ser
NM_003286.3:c.1768C>A (TOP1)	NP_003277.1:p.Arg590Ser
NM_003286.4:c.1768C>A (TOP1) MANE Select	NP_003277.1:p.Arg590Ser