Canonical Allele Identifier: CA409021916

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39745006A>C (hg19) ; chr20:g.41116366A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116366A>C , CM000682.2:g.41116366A>C	GRCh38
NC_000020.10:g.39745006A>C , CM000682.1:g.39745006A>C	GRCh37
NC_000020.9:g.39178420A>C	NCBI36
NG_012262.1:g.92545A>C
NG_012262.2:g.92545A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1796A>C (TOP1) MANE Select	ENSP00000354522.2:p.Gln599Pro
ENST00000680945.1:c.389A>C (TOP1)	ENSP00000504935.1:p.Gln130Pro
ENST00000681058.1:n.6582A>C (TOP1)
ENST00000681113.1:c.*1491A>C (TOP1)	ENSP00000505788.1:n.*1491A>C
ENST00000681392.1:n.3104A>C (TOP1)
ENST00000681884.1:n.3058A>C (TOP1)
ENST00000361337.2:c.1796A>C (TOP1)	ENSP00000354522.2:p.Gln599Pro
NM_003286.2:c.1796A>C (TOP1)	NP_003277.1:p.Gln599Pro
NR_109889.1:n.711-15077T>G (PLCG1-AS1)
XM_011529032.1:c.1292A>C (TOP1)	XP_011527334.1:p.Gln431Pro
XM_011529033.1:c.1058A>C (TOP1)	XP_011527335.1:p.Gln353Pro
NM_003286.3:c.1796A>C (TOP1)	NP_003277.1:p.Gln599Pro
NM_003286.4:c.1796A>C (TOP1) MANE Select	NP_003277.1:p.Gln599Pro