Canonical Allele Identifier: CA2652859358

Gene: TOP1 PLCG1-AS1

Linked Data

• gnomAD v4: 20-41116408-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116408C>A , CM000682.2:g.41116408C>A	GRCh38
NC_000020.10:g.39745048C>A , CM000682.1:g.39745048C>A	GRCh37
NC_000020.9:g.39178462C>A	NCBI36
NG_012262.1:g.92587C>A
NG_012262.2:g.92587C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1822+16C>A (TOP1) MANE Select	ENSP00000354522.2:n.1822+16C>A
ENST00000680945.1:c.415+16C>A (TOP1)	ENSP00000504935.1:n.415+16C>A
ENST00000681058.1:n.6608+16C>A (TOP1)
ENST00000681113.1:c.*1517+16C>A (TOP1)	ENSP00000505788.1:n.*1517+16C>A
ENST00000681392.1:n.3130+16C>A (TOP1)
ENST00000681884.1:n.3084+16C>A (TOP1)
ENST00000361337.2:c.1822+16C>A (TOP1)	ENSP00000354522.2:n.1822+16C>A
NM_003286.2:c.1822+16C>A (TOP1)	NP_003277.1:n.1822+16C>A
NR_109889.1:n.711-15119G>T (PLCG1-AS1)
XM_011529032.1:c.1318+16C>A (TOP1)	XP_011527334.1:n.1318+16C>A
XM_011529033.1:c.1084+16C>A (TOP1)	XP_011527335.1:n.1084+16C>A
NM_003286.3:c.1822+16C>A (TOP1)	NP_003277.1:n.1822+16C>A
NM_003286.4:c.1822+16C>A (TOP1) MANE Select	NP_003277.1:n.1822+16C>A