Canonical Allele Identifier: CA2652859351

Gene: TOP1 PLCG1-AS1

Linked Data

• gnomAD v4: 20-41116269-C-CATTAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116269_41116270insATTAAAAAA , CM000682.2:g.41116269_41116270insATTAAAAAA	GRCh38
NC_000020.10:g.39744909_39744910insATTAAAAAA , CM000682.1:g.39744909_39744910insATTAAAAAA	GRCh37
NC_000020.9:g.39178323_39178324insATTAAAAAA	NCBI36
NG_012262.1:g.92448_92449insATTAAAAAA
NG_012262.2:g.92448_92449insATTAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1708-9_1708-8insATTAAAAAA (TOP1) MANE Select	ENSP00000354522.2:n.1708-9_1708-8insATTAAAAAA
ENST00000680945.1:c.301-9_301-8insATTAAAAAA (TOP1)	ENSP00000504935.1:n.301-9_301-8insATTAAAAAA
ENST00000681058.1:n.6494-9_6494-8insATTAAAAAA (TOP1)
ENST00000681113.1:c.*1403-9_*1403-8insATTAAAAAA (TOP1)	ENSP00000505788.1:n.*1403-9_*1403-8insATTAAAAAA
ENST00000681392.1:n.3016-9_3016-8insATTAAAAAA (TOP1)
ENST00000681884.1:n.2970-9_2970-8insATTAAAAAA (TOP1)
ENST00000361337.2:c.1708-9_1708-8insATTAAAAAA (TOP1)	ENSP00000354522.2:n.1708-9_1708-8insATTAAAAAA
NM_003286.2:c.1708-9_1708-8insATTAAAAAA (TOP1)	NP_003277.1:n.1708-9_1708-8insATTAAAAAA
NR_109889.1:n.711-14981_711-14980insTTTTTTAAT (PLCG1-AS1)
XM_011529032.1:c.1204-9_1204-8insATTAAAAAA (TOP1)	XP_011527334.1:n.1204-9_1204-8insATTAAAAAA
XM_011529033.1:c.970-9_970-8insATTAAAAAA (TOP1)	XP_011527335.1:n.970-9_970-8insATTAAAAAA
NM_003286.3:c.1708-9_1708-8insATTAAAAAA (TOP1)	NP_003277.1:n.1708-9_1708-8insATTAAAAAA
NM_003286.4:c.1708-9_1708-8insATTAAAAAA (TOP1) MANE Select	NP_003277.1:n.1708-9_1708-8insATTAAAAAA