Canonical Allele Identifier: CA510555050

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744965A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116325A>C , CM000682.2:g.41116325A>C	GRCh38
NC_000020.10:g.39744965A>C , CM000682.1:g.39744965A>C	GRCh37
NC_000020.9:g.39178379A>C	NCBI36
NG_012262.1:g.92504A>C
NG_012262.2:g.92504A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361337.3:c.1755A>C (TOP1) MANE Select	ENSP00000354522.2:p.Thr585=
ENST00000680945.1:c.348A>C (TOP1)	ENSP00000504935.1:p.Thr116=
ENST00000681058.1:n.6541A>C (TOP1)
ENST00000681113.1:c.*1450A>C (TOP1)	ENSP00000505788.1:n.*1450A>C
ENST00000681392.1:n.3063A>C (TOP1)
ENST00000681884.1:n.3017A>C (TOP1)
ENST00000361337.2:c.1755A>C (TOP1)	ENSP00000354522.2:p.Thr585=
NM_003286.2:c.1755A>C (TOP1)	NP_003277.1:p.Thr585=
NR_109889.1:n.711-15036T>G (PLCG1-AS1)
XM_011529032.1:c.1251A>C (TOP1)	XP_011527334.1:p.Thr417=
XM_011529033.1:c.1017A>C (TOP1)	XP_011527335.1:p.Thr339=
NM_003286.3:c.1755A>C (TOP1)	NP_003277.1:p.Thr585=
NM_003286.4:c.1755A>C (TOP1) MANE Select	NP_003277.1:p.Thr585=