Canonical Allele Identifier: CA409021844

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744973T>C (hg19) ; chr20:g.41116333T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116333T>C , CM000682.2:g.41116333T>C	GRCh38
NC_000020.10:g.39744973T>C , CM000682.1:g.39744973T>C	GRCh37
NC_000020.9:g.39178387T>C	NCBI36
NG_012262.1:g.92512T>C
NG_012262.2:g.92512T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361337.3:c.1763T>C (TOP1) MANE Select	ENSP00000354522.2:p.Val588Ala
ENST00000680945.1:c.356T>C (TOP1)	ENSP00000504935.1:p.Val119Ala
ENST00000681058.1:n.6549T>C (TOP1)
ENST00000681113.1:c.*1458T>C (TOP1)	ENSP00000505788.1:n.*1458T>C
ENST00000681392.1:n.3071T>C (TOP1)
ENST00000681884.1:n.3025T>C (TOP1)
ENST00000361337.2:c.1763T>C (TOP1)	ENSP00000354522.2:p.Val588Ala
NM_003286.2:c.1763T>C (TOP1)	NP_003277.1:p.Val588Ala
NR_109889.1:n.711-15044A>G (PLCG1-AS1)
XM_011529032.1:c.1259T>C (TOP1)	XP_011527334.1:p.Val420Ala
XM_011529033.1:c.1025T>C (TOP1)	XP_011527335.1:p.Val342Ala
NM_003286.3:c.1763T>C (TOP1)	NP_003277.1:p.Val588Ala
NM_003286.4:c.1763T>C (TOP1) MANE Select	NP_003277.1:p.Val588Ala