Canonical Allele Identifier: CA2652859345

Gene: TOP1 PLCG1-AS1

Linked Data

• gnomAD v4: 20-41116259-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116259G>C , CM000682.2:g.41116259G>C	GRCh38
NC_000020.10:g.39744899G>C , CM000682.1:g.39744899G>C	GRCh37
NC_000020.9:g.39178313G>C	NCBI36
NG_012262.1:g.92438G>C
NG_012262.2:g.92438G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1708-19G>C (TOP1) MANE Select	ENSP00000354522.2:n.1708-19G>C
ENST00000680945.1:c.301-19G>C (TOP1)	ENSP00000504935.1:n.301-19G>C
ENST00000681058.1:n.6494-19G>C (TOP1)
ENST00000681113.1:c.*1403-19G>C (TOP1)	ENSP00000505788.1:n.*1403-19G>C
ENST00000681392.1:n.3016-19G>C (TOP1)
ENST00000681884.1:n.2970-19G>C (TOP1)
ENST00000361337.2:c.1708-19G>C (TOP1)	ENSP00000354522.2:n.1708-19G>C
NM_003286.2:c.1708-19G>C (TOP1)	NP_003277.1:n.1708-19G>C
NR_109889.1:n.711-14970C>G (PLCG1-AS1)
XM_011529032.1:c.1204-19G>C (TOP1)	XP_011527334.1:n.1204-19G>C
XM_011529033.1:c.970-19G>C (TOP1)	XP_011527335.1:n.970-19G>C
NM_003286.3:c.1708-19G>C (TOP1)	NP_003277.1:n.1708-19G>C
NM_003286.4:c.1708-19G>C (TOP1) MANE Select	NP_003277.1:n.1708-19G>C