Canonical Allele Identifier: CA083627

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744958G>G (hg19) ; chr20:g.41116318G>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116318G= , CM000682.2:g.41116318G=	GRCh38
NC_000020.10:g.39744958G= , CM000682.1:g.39744958G=	GRCh37
NC_000020.9:g.39178372G=	NCBI36
NG_012262.1:g.92497G=
NG_012262.2:g.92497G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1748G= (TOP1) MANE Select	ENSP00000354522.2:p.Gly583=
ENST00000680945.1:c.341G= (TOP1)	ENSP00000504935.1:p.Gly114=
ENST00000681058.1:n.6534G= (TOP1)
ENST00000681113.1:c.*1443G= (TOP1)	ENSP00000505788.1:n.*1443G=
ENST00000681392.1:n.3056G= (TOP1)
ENST00000681884.1:n.3010G= (TOP1)
ENST00000361337.2:c.1748G= (TOP1)	ENSP00000354522.2:p.Gly583=
NM_003286.2:c.1748G= (TOP1)	NP_003277.1:p.Gly583=
NR_109889.1:n.711-15029C= (PLCG1-AS1)
XM_011529032.1:c.1244G= (TOP1)	XP_011527334.1:p.Gly415=
XM_011529033.1:c.1010G= (TOP1)	XP_011527335.1:p.Gly337=
NM_003286.3:c.1748G= (TOP1)	NP_003277.1:p.Gly583=
NM_003286.4:c.1748G= (TOP1) MANE Select	NP_003277.1:p.Gly583=