Canonical Allele Identifier: CA409021835

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744970A>C (hg19) ; chr20:g.41116330A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116330A>C , CM000682.2:g.41116330A>C	GRCh38
NC_000020.10:g.39744970A>C , CM000682.1:g.39744970A>C	GRCh37
NC_000020.9:g.39178384A>C	NCBI36
NG_012262.1:g.92509A>C
NG_012262.2:g.92509A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361337.3:c.1760A>C (TOP1) MANE Select	ENSP00000354522.2:p.Lys587Thr
ENST00000680945.1:c.353A>C (TOP1)	ENSP00000504935.1:p.Lys118Thr
ENST00000681058.1:n.6546A>C (TOP1)
ENST00000681113.1:c.*1455A>C (TOP1)	ENSP00000505788.1:n.*1455A>C
ENST00000681392.1:n.3068A>C (TOP1)
ENST00000681884.1:n.3022A>C (TOP1)
ENST00000361337.2:c.1760A>C (TOP1)	ENSP00000354522.2:p.Lys587Thr
NM_003286.2:c.1760A>C (TOP1)	NP_003277.1:p.Lys587Thr
NR_109889.1:n.711-15041T>G (PLCG1-AS1)
XM_011529032.1:c.1256A>C (TOP1)	XP_011527334.1:p.Lys419Thr
XM_011529033.1:c.1022A>C (TOP1)	XP_011527335.1:p.Lys341Thr
NM_003286.3:c.1760A>C (TOP1)	NP_003277.1:p.Lys587Thr
NM_003286.4:c.1760A>C (TOP1) MANE Select	NP_003277.1:p.Lys587Thr