Canonical Allele Identifier: CA510555042

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744959C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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