Canonical Allele Identifier: CA2652859448

Gene: TOP1 PLCG1-AS1

Linked Data

• gnomAD v4: 20-41116538-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116538T>G , CM000682.2:g.41116538T>G	GRCh38
NC_000020.10:g.39745178T>G , CM000682.1:g.39745178T>G	GRCh37
NC_000020.9:g.39178592T>G	NCBI36
NG_012262.1:g.92717T>G
NG_012262.2:g.92717T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1822+146T>G (TOP1) MANE Select	ENSP00000354522.2:n.1822+146T>G
ENST00000680945.1:c.415+146T>G (TOP1)	ENSP00000504935.1:n.415+146T>G
ENST00000681058.1:n.6608+146T>G (TOP1)
ENST00000681113.1:c.*1517+146T>G (TOP1)	ENSP00000505788.1:n.*1517+146T>G
ENST00000681392.1:n.3130+146T>G (TOP1)
ENST00000681884.1:n.3084+146T>G (TOP1)
ENST00000361337.2:c.1822+146T>G (TOP1)	ENSP00000354522.2:n.1822+146T>G
NM_003286.2:c.1822+146T>G (TOP1)	NP_003277.1:n.1822+146T>G
NR_109889.1:n.711-15249A>C (PLCG1-AS1)
XM_011529032.1:c.1318+146T>G (TOP1)	XP_011527334.1:n.1318+146T>G
XM_011529033.1:c.1084+146T>G (TOP1)	XP_011527335.1:n.1084+146T>G
NM_003286.3:c.1822+146T>G (TOP1)	NP_003277.1:n.1822+146T>G
NM_003286.4:c.1822+146T>G (TOP1) MANE Select	NP_003277.1:n.1822+146T>G