Canonical Allele Identifier: CA2364230784

Gene: TOP1 PLCG1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116023_41116025delinsGAT , CM000682.2:g.41116023_41116025delinsGAT	GRCh38
NC_000020.10:g.39744663_39744665delinsGAT , CM000682.1:g.39744663_39744665delinsGAT	GRCh37
NC_000020.9:g.39178077_39178079delinsGAT	NCBI36
NG_012262.1:g.92202_92204delinsGAT
NG_012262.2:g.92202_92204delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1708-255_1708-253delinsGAT (TOP1) MANE Select	ENSP00000354522.2:n.1708-255_1708-253delinsGAT
ENST00000680945.1:c.301-255_301-253delinsGAT (TOP1)	ENSP00000504935.1:n.301-255_301-253delinsGAT
ENST00000681058.1:n.6494-255_6494-253delinsGAT (TOP1)
ENST00000681113.1:c.*1403-255_*1403-253delinsGAT (TOP1)	ENSP00000505788.1:n.*1403-255_*1403-253delinsGAT
ENST00000681392.1:n.3016-255_3016-253delinsGAT (TOP1)
ENST00000681884.1:n.2970-255_2970-253delinsGAT (TOP1)
ENST00000361337.2:c.1708-255_1708-253delinsGAT (TOP1)	ENSP00000354522.2:n.1708-255_1708-253delinsGAT
NM_003286.2:c.1708-255_1708-253delinsGAT (TOP1)	NP_003277.1:n.1708-255_1708-253delinsGAT
NR_109889.1:n.711-14736_711-14734delinsATC (PLCG1-AS1)
XM_011529032.1:c.1204-255_1204-253delinsGAT (TOP1)	XP_011527334.1:n.1204-255_1204-253delinsGAT
XM_011529033.1:c.970-255_970-253delinsGAT (TOP1)	XP_011527335.1:n.970-255_970-253delinsGAT
NM_003286.3:c.1708-255_1708-253delinsGAT (TOP1)	NP_003277.1:n.1708-255_1708-253delinsGAT
NM_003286.4:c.1708-255_1708-253delinsGAT (TOP1) MANE Select	NP_003277.1:n.1708-255_1708-253delinsGAT