Canonical Allele Identifier: CA233207
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs267607132

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41116318G>A , CM000682.2:g.41116318G>A GRCh38
NC_000020.10:g.39744958G>A , CM000682.1:g.39744958G>A GRCh37
NC_000020.9:g.39178372G>A NCBI36
NG_012262.1:g.92497G>A
NG_012262.2:g.92497G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361337.3:c.1748G>A (TOP1) MANE Select ENSP00000354522.2:p.Gly583Asp
ENST00000680945.1:c.341G>A (TOP1) ENSP00000504935.1:p.Gly114Asp
ENST00000681058.1:n.6534G>A (TOP1)
ENST00000681113.1:c.*1443G>A (TOP1) ENSP00000505788.1:n.*1443G>A
ENST00000681392.1:n.3056G>A (TOP1)
ENST00000681884.1:n.3010G>A (TOP1)
ENST00000361337.2:c.1748G>A (TOP1) ENSP00000354522.2:p.Gly583Asp
NM_003286.2:c.1748G>A (TOP1) NP_003277.1:p.Gly583Asp
NR_109889.1:n.711-15029C>T (PLCG1-AS1)
XM_011529032.1:c.1244G>A (TOP1) XP_011527334.1:p.Gly415Asp
XM_011529033.1:c.1010G>A (TOP1) XP_011527335.1:p.Gly337Asp
NM_003286.3:c.1748G>A (TOP1) NP_003277.1:p.Gly583Asp
NM_003286.4:c.1748G>A (TOP1) MANE Select NP_003277.1:p.Gly583Asp