Canonical Allele Identifier: CA2652859335

Gene: TOP1 PLCG1-AS1

Linked Data

• gnomAD v4: 20-41116238-GTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116241_41116242del , CM000682.2:g.41116241_41116242del	GRCh38
NC_000020.10:g.39744881_39744882del , CM000682.1:g.39744881_39744882del	GRCh37
NC_000020.9:g.39178295_39178296del	NCBI36
NG_012262.1:g.92420_92421del
NG_012262.2:g.92420_92421del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1708-37_1708-36del (TOP1) MANE Select	ENSP00000354522.2:n.1708-37_1708-36del
ENST00000680945.1:c.301-37_301-36del (TOP1)	ENSP00000504935.1:n.301-37_301-36del
ENST00000681058.1:n.6494-37_6494-36del (TOP1)
ENST00000681113.1:c.*1403-37_*1403-36del (TOP1)	ENSP00000505788.1:n.*1403-37_*1403-36del
ENST00000681392.1:n.3016-37_3016-36del (TOP1)
ENST00000681884.1:n.2970-37_2970-36del (TOP1)
ENST00000361337.2:c.1708-37_1708-36del (TOP1)	ENSP00000354522.2:n.1708-37_1708-36del
NM_003286.2:c.1708-37_1708-36del (TOP1)	NP_003277.1:n.1708-37_1708-36del
NR_109889.1:n.711-14951_711-14950del (PLCG1-AS1)
XM_011529032.1:c.1204-37_1204-36del (TOP1)	XP_011527334.1:n.1204-37_1204-36del
XM_011529033.1:c.970-37_970-36del (TOP1)	XP_011527335.1:n.970-37_970-36del
NM_003286.3:c.1708-37_1708-36del (TOP1)	NP_003277.1:n.1708-37_1708-36del
NM_003286.4:c.1708-37_1708-36del (TOP1) MANE Select	NP_003277.1:n.1708-37_1708-36del