Canonical Allele Identifier: CA409021770

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744942C>G (hg19) ; chr20:g.41116302C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116302C>G , CM000682.2:g.41116302C>G	GRCh38
NC_000020.10:g.39744942C>G , CM000682.1:g.39744942C>G	GRCh37
NC_000020.9:g.39178356C>G	NCBI36
NG_012262.1:g.92481C>G
NG_012262.2:g.92481C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1732C>G (TOP1) MANE Select	ENSP00000354522.2:p.Gln578Glu
ENST00000680945.1:c.325C>G (TOP1)	ENSP00000504935.1:p.Gln109Glu
ENST00000681058.1:n.6518C>G (TOP1)
ENST00000681113.1:c.*1427C>G (TOP1)	ENSP00000505788.1:n.*1427C>G
ENST00000681392.1:n.3040C>G (TOP1)
ENST00000681884.1:n.2994C>G (TOP1)
ENST00000361337.2:c.1732C>G (TOP1)	ENSP00000354522.2:p.Gln578Glu
NM_003286.2:c.1732C>G (TOP1)	NP_003277.1:p.Gln578Glu
NR_109889.1:n.711-15013G>C (PLCG1-AS1)
XM_011529032.1:c.1228C>G (TOP1)	XP_011527334.1:p.Gln410Glu
XM_011529033.1:c.994C>G (TOP1)	XP_011527335.1:p.Gln332Glu
NM_003286.3:c.1732C>G (TOP1)	NP_003277.1:p.Gln578Glu
NM_003286.4:c.1732C>G (TOP1) MANE Select	NP_003277.1:p.Gln578Glu