Canonical Allele Identifier: CA409021979

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39745034T>G (hg19) ; chr20:g.41116394T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116394T>G , CM000682.2:g.41116394T>G	GRCh38
NC_000020.10:g.39745034T>G , CM000682.1:g.39745034T>G	GRCh37
NC_000020.9:g.39178448T>G	NCBI36
NG_012262.1:g.92573T>G
NG_012262.2:g.92573T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1822+2T>G (TOP1) MANE Select	ENSP00000354522.2:n.1822+2T>G
ENST00000680945.1:c.415+2T>G (TOP1)	ENSP00000504935.1:n.415+2T>G
ENST00000681058.1:n.6608+2T>G (TOP1)
ENST00000681113.1:c.*1517+2T>G (TOP1)	ENSP00000505788.1:n.*1517+2T>G
ENST00000681392.1:n.3130+2T>G (TOP1)
ENST00000681884.1:n.3084+2T>G (TOP1)
ENST00000361337.2:c.1822+2T>G (TOP1)	ENSP00000354522.2:n.1822+2T>G
NM_003286.2:c.1822+2T>G (TOP1)	NP_003277.1:n.1822+2T>G
NR_109889.1:n.711-15105A>C (PLCG1-AS1)
XM_011529032.1:c.1318+2T>G (TOP1)	XP_011527334.1:n.1318+2T>G
XM_011529033.1:c.1084+2T>G (TOP1)	XP_011527335.1:n.1084+2T>G
NM_003286.3:c.1822+2T>G (TOP1)	NP_003277.1:n.1822+2T>G
NM_003286.4:c.1822+2T>G (TOP1) MANE Select	NP_003277.1:n.1822+2T>G