Canonical Allele Identifier: CA510555134

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39745028A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116388A>G , CM000682.2:g.41116388A>G	GRCh38
NC_000020.10:g.39745028A>G , CM000682.1:g.39745028A>G	GRCh37
NC_000020.9:g.39178442A>G	NCBI36
NG_012262.1:g.92567A>G
NG_012262.2:g.92567A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1818A>G (TOP1) MANE Select	ENSP00000354522.2:p.Thr606=
ENST00000680945.1:c.411A>G (TOP1)	ENSP00000504935.1:p.Thr137=
ENST00000681058.1:n.6604A>G (TOP1)
ENST00000681113.1:c.*1513A>G (TOP1)	ENSP00000505788.1:n.*1513A>G
ENST00000681392.1:n.3126A>G (TOP1)
ENST00000681884.1:n.3080A>G (TOP1)
ENST00000361337.2:c.1818A>G (TOP1)	ENSP00000354522.2:p.Thr606=
NM_003286.2:c.1818A>G (TOP1)	NP_003277.1:p.Thr606=
NR_109889.1:n.711-15099T>C (PLCG1-AS1)
XM_011529032.1:c.1314A>G (TOP1)	XP_011527334.1:p.Thr438=
XM_011529033.1:c.1080A>G (TOP1)	XP_011527335.1:p.Thr360=
NM_003286.3:c.1818A>G (TOP1)	NP_003277.1:p.Thr606=
NM_003286.4:c.1818A>G (TOP1) MANE Select	NP_003277.1:p.Thr606=