Canonical Allele Identifier: CA083614
Community Standard Title: NM_003286.4(TOP1):c.1598A>G (p.Asp533Gly)
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41114115A>G , CM000682.2:g.41114115A>G GRCh38
NC_000020.10:g.39742755A>G , CM000682.1:g.39742755A>G GRCh37
NC_000020.9:g.39176169A>G NCBI36
NG_012262.1:g.90294A>G
NG_012262.2:g.90294A>G

Transcript Alleles

HGVS Amino-acid Change
NM_003286.4:c.1598A>G (TOP1) MANE Select NP_003277.1:p.Asp533Gly
ENST00000361337.3:c.1598A>G (TOP1) MANE Select ENSP00000354522.2:p.Asp533Gly
NM_003286.2:c.1598A>G (TOP1) NP_003277.1:p.Asp533Gly
NM_003286.3:c.1598A>G (TOP1) NP_003277.1:p.Asp533Gly
NR_109889.1:n.711-12826T>C (PLCG1-AS1)
ENST00000361337.2:c.1598A>G (TOP1) ENSP00000354522.2:p.Asp533Gly
ENST00000680945.1:c.191A>G (TOP1) ENSP00000504935.1:p.Asp64Gly
ENST00000681058.1:n.6384A>G (TOP1)
ENST00000681113.1:c.*1293A>G (TOP1) ENSP00000505788.1:n.*1293A>G
ENST00000681392.1:n.2906A>G (TOP1)
ENST00000681884.1:n.2860A>G (TOP1)
XM_011529032.1:c.1094A>G (TOP1) XP_011527334.1:p.Asp365Gly
XM_011529033.1:c.860A>G (TOP1) XP_011527335.1:p.Asp287Gly