Canonical Allele Identifier: CA2364230917

Gene: TOP1 PLCG1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116367G= , CM000682.2:g.41116367G=	GRCh38
NC_000020.10:g.39745007G= , CM000682.1:g.39745007G=	GRCh37
NC_000020.9:g.39178421G=	NCBI36
NG_012262.1:g.92546G=
NG_012262.2:g.92546G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1797G= (TOP1) MANE Select	ENSP00000354522.2:p.Gln599=
ENST00000680945.1:c.390G= (TOP1)	ENSP00000504935.1:p.Gln130=
ENST00000681058.1:n.6583G= (TOP1)
ENST00000681113.1:c.*1492G= (TOP1)	ENSP00000505788.1:n.*1492G=
ENST00000681392.1:n.3105G= (TOP1)
ENST00000681884.1:n.3059G= (TOP1)
ENST00000361337.2:c.1797G= (TOP1)	ENSP00000354522.2:p.Gln599=
NM_003286.2:c.1797G= (TOP1)	NP_003277.1:p.Gln599=
NR_109889.1:n.711-15078C= (PLCG1-AS1)
XM_011529032.1:c.1293G= (TOP1)	XP_011527334.1:p.Gln431=
XM_011529033.1:c.1059G= (TOP1)	XP_011527335.1:p.Gln353=
NM_003286.3:c.1797G= (TOP1)	NP_003277.1:p.Gln599=
NM_003286.4:c.1797G= (TOP1) MANE Select	NP_003277.1:p.Gln599=