Canonical Allele Identifier: CA409021895

Gene: TOP1 PLCG1-AS1

Linked Data

• dbSNP Id: rs2034329301
• MyVariant Identifiers: chr20:g.39744996A>G (hg19) ; chr20:g.41116356A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116356A>G , CM000682.2:g.41116356A>G	GRCh38
NC_000020.10:g.39744996A>G , CM000682.1:g.39744996A>G	GRCh37
NC_000020.9:g.39178410A>G	NCBI36
NG_012262.1:g.92535A>G
NG_012262.2:g.92535A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1786A>G (TOP1) MANE Select	ENSP00000354522.2:p.Ile596Val
ENST00000680945.1:c.379A>G (TOP1)	ENSP00000504935.1:p.Ile127Val
ENST00000681058.1:n.6572A>G (TOP1)
ENST00000681113.1:c.*1481A>G (TOP1)	ENSP00000505788.1:n.*1481A>G
ENST00000681392.1:n.3094A>G (TOP1)
ENST00000681884.1:n.3048A>G (TOP1)
ENST00000361337.2:c.1786A>G (TOP1)	ENSP00000354522.2:p.Ile596Val
NM_003286.2:c.1786A>G (TOP1)	NP_003277.1:p.Ile596Val
NR_109889.1:n.711-15067T>C (PLCG1-AS1)
XM_011529032.1:c.1282A>G (TOP1)	XP_011527334.1:p.Ile428Val
XM_011529033.1:c.1048A>G (TOP1)	XP_011527335.1:p.Ile350Val
NM_003286.3:c.1786A>G (TOP1)	NP_003277.1:p.Ile596Val
NM_003286.4:c.1786A>G (TOP1) MANE Select	NP_003277.1:p.Ile596Val