Canonical Allele Identifier: CA510555043
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Linked Data

COSMIC: COSM118370
MyVariant Identifiers: chr20:g.39744959C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41116319C>G , CM000682.2:g.41116319C>G GRCh38
NC_000020.10:g.39744959C>G , CM000682.1:g.39744959C>G GRCh37
NC_000020.9:g.39178373C>G NCBI36
NG_012262.1:g.92498C>G
NG_012262.2:g.92498C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361337.3:c.1749C>G (TOP1) MANE Select ENSP00000354522.2:p.Gly583=
ENST00000680945.1:c.342C>G (TOP1) ENSP00000504935.1:p.Gly114=
ENST00000681058.1:n.6535C>G (TOP1)
ENST00000681113.1:c.*1444C>G (TOP1) ENSP00000505788.1:n.*1444C>G
ENST00000681392.1:n.3057C>G (TOP1)
ENST00000681884.1:n.3011C>G (TOP1)
ENST00000361337.2:c.1749C>G (TOP1) ENSP00000354522.2:p.Gly583=
NM_003286.2:c.1749C>G (TOP1) NP_003277.1:p.Gly583=
NR_109889.1:n.711-15030G>C (PLCG1-AS1)
XM_011529032.1:c.1245C>G (TOP1) XP_011527334.1:p.Gly415=
XM_011529033.1:c.1011C>G (TOP1) XP_011527335.1:p.Gly337=
NM_003286.3:c.1749C>G (TOP1) NP_003277.1:p.Gly583=
NM_003286.4:c.1749C>G (TOP1) MANE Select NP_003277.1:p.Gly583=