Canonical Allele Identifier: CA2652859332

Gene: TOP1 PLCG1-AS1

Linked Data

• gnomAD v4: 20-41116236-T-TAG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116237_41116238dup , CM000682.2:g.41116237_41116238dup	GRCh38
NC_000020.10:g.39744877_39744878dup , CM000682.1:g.39744877_39744878dup	GRCh37
NC_000020.9:g.39178291_39178292dup	NCBI36
NG_012262.1:g.92416_92417dup
NG_012262.2:g.92416_92417dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1708-41_1708-40dup (TOP1) MANE Select	ENSP00000354522.2:n.1708-41_1708-40dup
ENST00000680945.1:c.301-41_301-40dup (TOP1)	ENSP00000504935.1:n.301-41_301-40dup
ENST00000681058.1:n.6494-41_6494-40dup (TOP1)
ENST00000681113.1:c.*1403-41_*1403-40dup (TOP1)	ENSP00000505788.1:n.*1403-41_*1403-40dup
ENST00000681392.1:n.3016-41_3016-40dup (TOP1)
ENST00000681884.1:n.2970-41_2970-40dup (TOP1)
ENST00000361337.2:c.1708-41_1708-40dup (TOP1)	ENSP00000354522.2:n.1708-41_1708-40dup
NM_003286.2:c.1708-41_1708-40dup (TOP1)	NP_003277.1:n.1708-41_1708-40dup
NR_109889.1:n.711-14949_711-14948dup (PLCG1-AS1)
XM_011529032.1:c.1204-41_1204-40dup (TOP1)	XP_011527334.1:n.1204-41_1204-40dup
XM_011529033.1:c.970-41_970-40dup (TOP1)	XP_011527335.1:n.970-41_970-40dup
NM_003286.3:c.1708-41_1708-40dup (TOP1)	NP_003277.1:n.1708-41_1708-40dup
NM_003286.4:c.1708-41_1708-40dup (TOP1) MANE Select	NP_003277.1:n.1708-41_1708-40dup