Canonical Allele Identifier: CA2364230756

Gene: TOP1 PLCG1-AS1

Linked Data

• dbSNP Id: rs2034322786

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41115974_41115975insTA , CM000682.2:g.41115974_41115975insTA	GRCh38
NC_000020.10:g.39744614_39744615insTA , CM000682.1:g.39744614_39744615insTA	GRCh37
NC_000020.9:g.39178028_39178029insTA	NCBI36
NG_012262.1:g.92153_92154insTA
NG_012262.2:g.92153_92154insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1708-304_1708-303insTA (TOP1) MANE Select	ENSP00000354522.2:n.1708-304_1708-303insTA
ENST00000680945.1:c.301-304_301-303insTA (TOP1)	ENSP00000504935.1:n.301-304_301-303insTA
ENST00000681058.1:n.6494-304_6494-303insTA (TOP1)
ENST00000681113.1:c.*1403-304_*1403-303insTA (TOP1)	ENSP00000505788.1:n.*1403-304_*1403-303insTA
ENST00000681392.1:n.3016-304_3016-303insTA (TOP1)
ENST00000681884.1:n.2970-304_2970-303insTA (TOP1)
ENST00000361337.2:c.1708-304_1708-303insTA (TOP1)	ENSP00000354522.2:n.1708-304_1708-303insTA
NM_003286.2:c.1708-304_1708-303insTA (TOP1)	NP_003277.1:n.1708-304_1708-303insTA
NR_109889.1:n.711-14686_711-14685insTA (PLCG1-AS1)
XM_011529032.1:c.1204-304_1204-303insTA (TOP1)	XP_011527334.1:n.1204-304_1204-303insTA
XM_011529033.1:c.970-304_970-303insTA (TOP1)	XP_011527335.1:n.970-304_970-303insTA
NM_003286.3:c.1708-304_1708-303insTA (TOP1)	NP_003277.1:n.1708-304_1708-303insTA
NM_003286.4:c.1708-304_1708-303insTA (TOP1) MANE Select	NP_003277.1:n.1708-304_1708-303insTA