Canonical Allele Identifier: CA409021734

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744926T>G (hg19) ; chr20:g.41116286T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116286T>G , CM000682.2:g.41116286T>G	GRCh38
NC_000020.10:g.39744926T>G , CM000682.1:g.39744926T>G	GRCh37
NC_000020.9:g.39178340T>G	NCBI36
NG_012262.1:g.92465T>G
NG_012262.2:g.92465T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1716T>G (TOP1) MANE Select	ENSP00000354522.2:p.Ile572Met
ENST00000680945.1:c.309T>G (TOP1)	ENSP00000504935.1:p.Ile103Met
ENST00000681058.1:n.6502T>G (TOP1)
ENST00000681113.1:c.*1411T>G (TOP1)	ENSP00000505788.1:n.*1411T>G
ENST00000681392.1:n.3024T>G (TOP1)
ENST00000681884.1:n.2978T>G (TOP1)
ENST00000361337.2:c.1716T>G (TOP1)	ENSP00000354522.2:p.Ile572Met
NM_003286.2:c.1716T>G (TOP1)	NP_003277.1:p.Ile572Met
NR_109889.1:n.711-14997A>C (PLCG1-AS1)
XM_011529032.1:c.1212T>G (TOP1)	XP_011527334.1:p.Ile404Met
XM_011529033.1:c.978T>G (TOP1)	XP_011527335.1:p.Ile326Met
NM_003286.3:c.1716T>G (TOP1)	NP_003277.1:p.Ile572Met
NM_003286.4:c.1716T>G (TOP1) MANE Select	NP_003277.1:p.Ile572Met