Canonical Allele Identifier: CA2364231007

Gene: TOP1 PLCG1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116562G= , CM000682.2:g.41116562G=	GRCh38
NC_000020.10:g.39745202G= , CM000682.1:g.39745202G=	GRCh37
NC_000020.9:g.39178616G=	NCBI36
NG_012262.1:g.92741G=
NG_012262.2:g.92741G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1822+170G= (TOP1) MANE Select	ENSP00000354522.2:n.1822+170G=
ENST00000680945.1:c.415+170G= (TOP1)	ENSP00000504935.1:n.415+170G=
ENST00000681058.1:n.6608+170G= (TOP1)
ENST00000681113.1:c.*1517+170G= (TOP1)	ENSP00000505788.1:n.*1517+170G=
ENST00000681392.1:n.3130+170G= (TOP1)
ENST00000681884.1:n.3084+170G= (TOP1)
ENST00000361337.2:c.1822+170G= (TOP1)	ENSP00000354522.2:n.1822+170G=
NM_003286.2:c.1822+170G= (TOP1)	NP_003277.1:n.1822+170G=
NR_109889.1:n.711-15273C= (PLCG1-AS1)
XM_011529032.1:c.1318+170G= (TOP1)	XP_011527334.1:n.1318+170G=
XM_011529033.1:c.1084+170G= (TOP1)	XP_011527335.1:n.1084+170G=
NM_003286.3:c.1822+170G= (TOP1)	NP_003277.1:n.1822+170G=
NM_003286.4:c.1822+170G= (TOP1) MANE Select	NP_003277.1:n.1822+170G=