Canonical Allele Identifier: CA409021930

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39745012A>C (hg19) ; chr20:g.41116372A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116372A>C , CM000682.2:g.41116372A>C	GRCh38
NC_000020.10:g.39745012A>C , CM000682.1:g.39745012A>C	GRCh37
NC_000020.9:g.39178426A>C	NCBI36
NG_012262.1:g.92551A>C
NG_012262.2:g.92551A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1802A>C (TOP1) MANE Select	ENSP00000354522.2:p.Gln601Pro
ENST00000680945.1:c.395A>C (TOP1)	ENSP00000504935.1:p.Gln132Pro
ENST00000681058.1:n.6588A>C (TOP1)
ENST00000681113.1:c.*1497A>C (TOP1)	ENSP00000505788.1:n.*1497A>C
ENST00000681392.1:n.3110A>C (TOP1)
ENST00000681884.1:n.3064A>C (TOP1)
ENST00000361337.2:c.1802A>C (TOP1)	ENSP00000354522.2:p.Gln601Pro
NM_003286.2:c.1802A>C (TOP1)	NP_003277.1:p.Gln601Pro
NR_109889.1:n.711-15083T>G (PLCG1-AS1)
XM_011529032.1:c.1298A>C (TOP1)	XP_011527334.1:p.Gln433Pro
XM_011529033.1:c.1064A>C (TOP1)	XP_011527335.1:p.Gln355Pro
NM_003286.3:c.1802A>C (TOP1)	NP_003277.1:p.Gln601Pro
NM_003286.4:c.1802A>C (TOP1) MANE Select	NP_003277.1:p.Gln601Pro