Canonical Allele Identifier: CA409021905

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39745000C>G (hg19) ; chr20:g.41116360C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116360C>G , CM000682.2:g.41116360C>G	GRCh38
NC_000020.10:g.39745000C>G , CM000682.1:g.39745000C>G	GRCh37
NC_000020.9:g.39178414C>G	NCBI36
NG_012262.1:g.92539C>G
NG_012262.2:g.92539C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1790C>G (TOP1) MANE Select	ENSP00000354522.2:p.Thr597Arg
ENST00000680945.1:c.383C>G (TOP1)	ENSP00000504935.1:p.Thr128Arg
ENST00000681058.1:n.6576C>G (TOP1)
ENST00000681113.1:c.*1485C>G (TOP1)	ENSP00000505788.1:n.*1485C>G
ENST00000681392.1:n.3098C>G (TOP1)
ENST00000681884.1:n.3052C>G (TOP1)
ENST00000361337.2:c.1790C>G (TOP1)	ENSP00000354522.2:p.Thr597Arg
NM_003286.2:c.1790C>G (TOP1)	NP_003277.1:p.Thr597Arg
NR_109889.1:n.711-15071G>C (PLCG1-AS1)
XM_011529032.1:c.1286C>G (TOP1)	XP_011527334.1:p.Thr429Arg
XM_011529033.1:c.1052C>G (TOP1)	XP_011527335.1:p.Thr351Arg
NM_003286.3:c.1790C>G (TOP1)	NP_003277.1:p.Thr597Arg
NM_003286.4:c.1790C>G (TOP1) MANE Select	NP_003277.1:p.Thr597Arg