Canonical Allele Identifier: CA2652859303

Gene: TOP1 PLCG1-AS1

Linked Data

• gnomAD v4: 20-41116189-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116189T>C , CM000682.2:g.41116189T>C	GRCh38
NC_000020.10:g.39744829T>C , CM000682.1:g.39744829T>C	GRCh37
NC_000020.9:g.39178243T>C	NCBI36
NG_012262.1:g.92368T>C
NG_012262.2:g.92368T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1708-89T>C (TOP1) MANE Select	ENSP00000354522.2:n.1708-89T>C
ENST00000680945.1:c.301-89T>C (TOP1)	ENSP00000504935.1:n.301-89T>C
ENST00000681058.1:n.6494-89T>C (TOP1)
ENST00000681113.1:c.*1403-89T>C (TOP1)	ENSP00000505788.1:n.*1403-89T>C
ENST00000681392.1:n.3016-89T>C (TOP1)
ENST00000681884.1:n.2970-89T>C (TOP1)
ENST00000361337.2:c.1708-89T>C (TOP1)	ENSP00000354522.2:n.1708-89T>C
NM_003286.2:c.1708-89T>C (TOP1)	NP_003277.1:n.1708-89T>C
NR_109889.1:n.711-14900A>G (PLCG1-AS1)
XM_011529032.1:c.1204-89T>C (TOP1)	XP_011527334.1:n.1204-89T>C
XM_011529033.1:c.970-89T>C (TOP1)	XP_011527335.1:n.970-89T>C
NM_003286.3:c.1708-89T>C (TOP1)	NP_003277.1:n.1708-89T>C
NM_003286.4:c.1708-89T>C (TOP1) MANE Select	NP_003277.1:n.1708-89T>C