Canonical Allele Identifier: CA314495756

Gene: TOP1 PLCG1-AS1

Linked Data

• dbSNP Id: rs565150761
• MyVariant Identifiers: chr20:g.39744658A>G (hg19) ; chr20:g.41116018A>G (hg38)
• PubMed: PMID:24974849

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116018A>G , CM000682.2:g.41116018A>G	GRCh38
NC_000020.10:g.39744658A>G , CM000682.1:g.39744658A>G	GRCh37
NC_000020.9:g.39178072A>G	NCBI36
NG_012262.1:g.92197A>G
NG_012262.2:g.92197A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1708-260A>G (TOP1) MANE Select	ENSP00000354522.2:n.1708-260A>G
ENST00000680945.1:c.301-260A>G (TOP1)	ENSP00000504935.1:n.301-260A>G
ENST00000681058.1:n.6494-260A>G (TOP1)
ENST00000681113.1:c.*1403-260A>G (TOP1)	ENSP00000505788.1:n.*1403-260A>G
ENST00000681392.1:n.3016-260A>G (TOP1)
ENST00000681884.1:n.2970-260A>G (TOP1)
ENST00000361337.2:c.1708-260A>G (TOP1)	ENSP00000354522.2:n.1708-260A>G
NM_003286.2:c.1708-260A>G (TOP1)	NP_003277.1:n.1708-260A>G
NR_109889.1:n.711-14729T>C (PLCG1-AS1)
XM_011529032.1:c.1204-260A>G (TOP1)	XP_011527334.1:n.1204-260A>G
XM_011529033.1:c.970-260A>G (TOP1)	XP_011527335.1:n.970-260A>G
NM_003286.3:c.1708-260A>G (TOP1)	NP_003277.1:n.1708-260A>G
NM_003286.4:c.1708-260A>G (TOP1) MANE Select	NP_003277.1:n.1708-260A>G