Canonical Allele Identifier: CA2577489269
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Linked Data

gnomAD v4: 20-41116251-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41116251C>A , CM000682.2:g.41116251C>A GRCh38
NC_000020.10:g.39744891C>A , CM000682.1:g.39744891C>A GRCh37
NC_000020.9:g.39178305C>A NCBI36
NG_012262.1:g.92430C>A
NG_012262.2:g.92430C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361337.3:c.1708-27C>A (TOP1) MANE Select ENSP00000354522.2:n.1708-27C>A
ENST00000680945.1:c.301-27C>A (TOP1) ENSP00000504935.1:n.301-27C>A
ENST00000681058.1:n.6494-27C>A (TOP1)
ENST00000681113.1:c.*1403-27C>A (TOP1) ENSP00000505788.1:n.*1403-27C>A
ENST00000681392.1:n.3016-27C>A (TOP1)
ENST00000681884.1:n.2970-27C>A (TOP1)
ENST00000361337.2:c.1708-27C>A (TOP1) ENSP00000354522.2:n.1708-27C>A
NM_003286.2:c.1708-27C>A (TOP1) NP_003277.1:n.1708-27C>A
NR_109889.1:n.711-14962G>T (PLCG1-AS1)
XM_011529032.1:c.1204-27C>A (TOP1) XP_011527334.1:n.1204-27C>A
XM_011529033.1:c.970-27C>A (TOP1) XP_011527335.1:n.970-27C>A
NM_003286.3:c.1708-27C>A (TOP1) NP_003277.1:n.1708-27C>A
NM_003286.4:c.1708-27C>A (TOP1) MANE Select NP_003277.1:n.1708-27C>A
Search 100 bp 5'
Search 100 bp 3'