Canonical Allele Identifier: CA510555141

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39745031C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116391C>G , CM000682.2:g.41116391C>G	GRCh38
NC_000020.10:g.39745031C>G , CM000682.1:g.39745031C>G	GRCh37
NC_000020.9:g.39178445C>G	NCBI36
NG_012262.1:g.92570C>G
NG_012262.2:g.92570C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1821C>G (TOP1) MANE Select	ENSP00000354522.2:p.Ala607=
ENST00000680945.1:c.414C>G (TOP1)	ENSP00000504935.1:p.Ala138=
ENST00000681058.1:n.6607C>G (TOP1)
ENST00000681113.1:c.*1516C>G (TOP1)	ENSP00000505788.1:n.*1516C>G
ENST00000681392.1:n.3129C>G (TOP1)
ENST00000681884.1:n.3083C>G (TOP1)
ENST00000361337.2:c.1821C>G (TOP1)	ENSP00000354522.2:p.Ala607=
NM_003286.2:c.1821C>G (TOP1)	NP_003277.1:p.Ala607=
NR_109889.1:n.711-15102G>C (PLCG1-AS1)
XM_011529032.1:c.1317C>G (TOP1)	XP_011527334.1:p.Ala439=
XM_011529033.1:c.1083C>G (TOP1)	XP_011527335.1:p.Ala361=
NM_003286.3:c.1821C>G (TOP1)	NP_003277.1:p.Ala607=
NM_003286.4:c.1821C>G (TOP1) MANE Select	NP_003277.1:p.Ala607=