Canonical Allele Identifier: CA409021933

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39745013G>C (hg19) ; chr20:g.41116373G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116373G>C , CM000682.2:g.41116373G>C	GRCh38
NC_000020.10:g.39745013G>C , CM000682.1:g.39745013G>C	GRCh37
NC_000020.9:g.39178427G>C	NCBI36
NG_012262.1:g.92552G>C
NG_012262.2:g.92552G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1803G>C (TOP1) MANE Select	ENSP00000354522.2:p.Gln601His
ENST00000680945.1:c.396G>C (TOP1)	ENSP00000504935.1:p.Gln132His
ENST00000681058.1:n.6589G>C (TOP1)
ENST00000681113.1:c.*1498G>C (TOP1)	ENSP00000505788.1:n.*1498G>C
ENST00000681392.1:n.3111G>C (TOP1)
ENST00000681884.1:n.3065G>C (TOP1)
ENST00000361337.2:c.1803G>C (TOP1)	ENSP00000354522.2:p.Gln601His
NM_003286.2:c.1803G>C (TOP1)	NP_003277.1:p.Gln601His
NR_109889.1:n.711-15084C>G (PLCG1-AS1)
XM_011529032.1:c.1299G>C (TOP1)	XP_011527334.1:p.Gln433His
XM_011529033.1:c.1065G>C (TOP1)	XP_011527335.1:p.Gln355His
NM_003286.3:c.1803G>C (TOP1)	NP_003277.1:p.Gln601His
NM_003286.4:c.1803G>C (TOP1) MANE Select	NP_003277.1:p.Gln601His