Canonical Allele Identifier: CA409021951

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39745021A>C (hg19) ; chr20:g.41116381A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116381A>C , CM000682.2:g.41116381A>C	GRCh38
NC_000020.10:g.39745021A>C , CM000682.1:g.39745021A>C	GRCh37
NC_000020.9:g.39178435A>C	NCBI36
NG_012262.1:g.92560A>C
NG_012262.2:g.92560A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1811A>C (TOP1) MANE Select	ENSP00000354522.2:p.Glu604Ala
ENST00000680945.1:c.404A>C (TOP1)	ENSP00000504935.1:p.Glu135Ala
ENST00000681058.1:n.6597A>C (TOP1)
ENST00000681113.1:c.*1506A>C (TOP1)	ENSP00000505788.1:n.*1506A>C
ENST00000681392.1:n.3119A>C (TOP1)
ENST00000681884.1:n.3073A>C (TOP1)
ENST00000361337.2:c.1811A>C (TOP1)	ENSP00000354522.2:p.Glu604Ala
NM_003286.2:c.1811A>C (TOP1)	NP_003277.1:p.Glu604Ala
NR_109889.1:n.711-15092T>G (PLCG1-AS1)
XM_011529032.1:c.1307A>C (TOP1)	XP_011527334.1:p.Glu436Ala
XM_011529033.1:c.1073A>C (TOP1)	XP_011527335.1:p.Glu358Ala
NM_003286.3:c.1811A>C (TOP1)	NP_003277.1:p.Glu604Ala
NM_003286.4:c.1811A>C (TOP1) MANE Select	NP_003277.1:p.Glu604Ala