Canonical Allele Identifier: CA2364230920
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41116379A= , CM000682.2:g.41116379A= GRCh38
NC_000020.10:g.39745019A= , CM000682.1:g.39745019A= GRCh37
NC_000020.9:g.39178433A= NCBI36
NG_012262.1:g.92558A=
NG_012262.2:g.92558A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361337.3:c.1809A= (TOP1) MANE Select ENSP00000354522.2:p.Lys603=
ENST00000680945.1:c.402A= (TOP1) ENSP00000504935.1:p.Lys134=
ENST00000681058.1:n.6595A= (TOP1)
ENST00000681113.1:c.*1504A= (TOP1) ENSP00000505788.1:n.*1504A=
ENST00000681392.1:n.3117A= (TOP1)
ENST00000681884.1:n.3071A= (TOP1)
ENST00000361337.2:c.1809A= (TOP1) ENSP00000354522.2:p.Lys603=
NM_003286.2:c.1809A= (TOP1) NP_003277.1:p.Lys603=
NR_109889.1:n.711-15090T= (PLCG1-AS1)
XM_011529032.1:c.1305A= (TOP1) XP_011527334.1:p.Lys435=
XM_011529033.1:c.1071A= (TOP1) XP_011527335.1:p.Lys357=
NM_003286.3:c.1809A= (TOP1) NP_003277.1:p.Lys603=
NM_003286.4:c.1809A= (TOP1) MANE Select NP_003277.1:p.Lys603=