Canonical Allele Identifier: CA2364230922

Gene: TOP1 PLCG1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116389G= , CM000682.2:g.41116389G=	GRCh38
NC_000020.10:g.39745029G= , CM000682.1:g.39745029G=	GRCh37
NC_000020.9:g.39178443G=	NCBI36
NG_012262.1:g.92568G=
NG_012262.2:g.92568G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1819G= (TOP1) MANE Select	ENSP00000354522.2:p.Ala607=
ENST00000680945.1:c.412G= (TOP1)	ENSP00000504935.1:p.Ala138=
ENST00000681058.1:n.6605G= (TOP1)
ENST00000681113.1:c.*1514G= (TOP1)	ENSP00000505788.1:n.*1514G=
ENST00000681392.1:n.3127G= (TOP1)
ENST00000681884.1:n.3081G= (TOP1)
ENST00000361337.2:c.1819G= (TOP1)	ENSP00000354522.2:p.Ala607=
NM_003286.2:c.1819G= (TOP1)	NP_003277.1:p.Ala607=
NR_109889.1:n.711-15100C= (PLCG1-AS1)
XM_011529032.1:c.1315G= (TOP1)	XP_011527334.1:p.Ala439=
XM_011529033.1:c.1081G= (TOP1)	XP_011527335.1:p.Ala361=
NM_003286.3:c.1819G= (TOP1)	NP_003277.1:p.Ala607=
NM_003286.4:c.1819G= (TOP1) MANE Select	NP_003277.1:p.Ala607=