Canonical Allele Identifier: CA2364230998

Gene: TOP1 PLCG1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116542_41116543delinsGC , CM000682.2:g.41116542_41116543delinsGC	GRCh38
NC_000020.10:g.39745182_39745183delinsGC , CM000682.1:g.39745182_39745183delinsGC	GRCh37
NC_000020.9:g.39178596_39178597delinsGC	NCBI36
NG_012262.1:g.92721_92722delinsGC
NG_012262.2:g.92721_92722delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1822+150_1822+151delinsGC (TOP1) MANE Select	ENSP00000354522.2:n.1822+150_1822+151delinsGC
ENST00000680945.1:c.415+150_415+151delinsGC (TOP1)	ENSP00000504935.1:n.415+150_415+151delinsGC
ENST00000681058.1:n.6608+150_6608+151delinsGC (TOP1)
ENST00000681113.1:c.*1517+150_*1517+151delinsGC (TOP1)	ENSP00000505788.1:n.*1517+150_*1517+151delinsGC
ENST00000681392.1:n.3130+150_3130+151delinsGC (TOP1)
ENST00000681884.1:n.3084+150_3084+151delinsGC (TOP1)
ENST00000361337.2:c.1822+150_1822+151delinsGC (TOP1)	ENSP00000354522.2:n.1822+150_1822+151delinsGC
NM_003286.2:c.1822+150_1822+151delinsGC (TOP1)	NP_003277.1:n.1822+150_1822+151delinsGC
NR_109889.1:n.711-15254_711-15253delinsGC (PLCG1-AS1)
XM_011529032.1:c.1318+150_1318+151delinsGC (TOP1)	XP_011527334.1:n.1318+150_1318+151delinsGC
XM_011529033.1:c.1084+150_1084+151delinsGC (TOP1)	XP_011527335.1:n.1084+150_1084+151delinsGC
NM_003286.3:c.1822+150_1822+151delinsGC (TOP1)	NP_003277.1:n.1822+150_1822+151delinsGC
NM_003286.4:c.1822+150_1822+151delinsGC (TOP1) MANE Select	NP_003277.1:n.1822+150_1822+151delinsGC