Canonical Allele Identifier: CA2364230903
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41116295G= , CM000682.2:g.41116295G= GRCh38
NC_000020.10:g.39744935G= , CM000682.1:g.39744935G= GRCh37
NC_000020.9:g.39178349G= NCBI36
NG_012262.1:g.92474G=
NG_012262.2:g.92474G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361337.3:c.1725G= (TOP1) MANE Select ENSP00000354522.2:p.Lys575=
ENST00000680945.1:c.318G= (TOP1) ENSP00000504935.1:p.Lys106=
ENST00000681058.1:n.6511G= (TOP1)
ENST00000681113.1:c.*1420G= (TOP1) ENSP00000505788.1:n.*1420G=
ENST00000681392.1:n.3033G= (TOP1)
ENST00000681884.1:n.2987G= (TOP1)
ENST00000361337.2:c.1725G= (TOP1) ENSP00000354522.2:p.Lys575=
NM_003286.2:c.1725G= (TOP1) NP_003277.1:p.Lys575=
NR_109889.1:n.711-15006C= (PLCG1-AS1)
XM_011529032.1:c.1221G= (TOP1) XP_011527334.1:p.Lys407=
XM_011529033.1:c.987G= (TOP1) XP_011527335.1:p.Lys329=
NM_003286.3:c.1725G= (TOP1) NP_003277.1:p.Lys575=
NM_003286.4:c.1725G= (TOP1) MANE Select NP_003277.1:p.Lys575=