Canonical Allele Identifier: CA409021859

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744979G>T (hg19) ; chr20:g.41116339G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116339G>T , CM000682.2:g.41116339G>T	GRCh38
NC_000020.10:g.39744979G>T , CM000682.1:g.39744979G>T	GRCh37
NC_000020.9:g.39178393G>T	NCBI36
NG_012262.1:g.92518G>T
NG_012262.2:g.92518G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361337.3:c.1769G>T (TOP1) MANE Select	ENSP00000354522.2:p.Arg590Leu
ENST00000680945.1:c.362G>T (TOP1)	ENSP00000504935.1:p.Arg121Leu
ENST00000681058.1:n.6555G>T (TOP1)
ENST00000681113.1:c.*1464G>T (TOP1)	ENSP00000505788.1:n.*1464G>T
ENST00000681392.1:n.3077G>T (TOP1)
ENST00000681884.1:n.3031G>T (TOP1)
ENST00000361337.2:c.1769G>T (TOP1)	ENSP00000354522.2:p.Arg590Leu
NM_003286.2:c.1769G>T (TOP1)	NP_003277.1:p.Arg590Leu
NR_109889.1:n.711-15050C>A (PLCG1-AS1)
XM_011529032.1:c.1265G>T (TOP1)	XP_011527334.1:p.Arg422Leu
XM_011529033.1:c.1031G>T (TOP1)	XP_011527335.1:p.Arg344Leu
NM_003286.3:c.1769G>T (TOP1)	NP_003277.1:p.Arg590Leu
NM_003286.4:c.1769G>T (TOP1) MANE Select	NP_003277.1:p.Arg590Leu