Canonical Allele Identifier: CA409021780

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744946A>C (hg19) ; chr20:g.41116306A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116306A>C , CM000682.2:g.41116306A>C	GRCh38
NC_000020.10:g.39744946A>C , CM000682.1:g.39744946A>C	GRCh37
NC_000020.9:g.39178360A>C	NCBI36
NG_012262.1:g.92485A>C
NG_012262.2:g.92485A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1736A>C (TOP1) MANE Select	ENSP00000354522.2:p.Asp579Ala
ENST00000680945.1:c.329A>C (TOP1)	ENSP00000504935.1:p.Asp110Ala
ENST00000681058.1:n.6522A>C (TOP1)
ENST00000681113.1:c.*1431A>C (TOP1)	ENSP00000505788.1:n.*1431A>C
ENST00000681392.1:n.3044A>C (TOP1)
ENST00000681884.1:n.2998A>C (TOP1)
ENST00000361337.2:c.1736A>C (TOP1)	ENSP00000354522.2:p.Asp579Ala
NM_003286.2:c.1736A>C (TOP1)	NP_003277.1:p.Asp579Ala
NR_109889.1:n.711-15017T>G (PLCG1-AS1)
XM_011529032.1:c.1232A>C (TOP1)	XP_011527334.1:p.Asp411Ala
XM_011529033.1:c.998A>C (TOP1)	XP_011527335.1:p.Asp333Ala
NM_003286.3:c.1736A>C (TOP1)	NP_003277.1:p.Asp579Ala
NM_003286.4:c.1736A>C (TOP1) MANE Select	NP_003277.1:p.Asp579Ala