Canonical Allele Identifier: CA2364230923

Gene: TOP1 PLCG1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116392C= , CM000682.2:g.41116392C=	GRCh38
NC_000020.10:g.39745032C= , CM000682.1:g.39745032C=	GRCh37
NC_000020.9:g.39178446C=	NCBI36
NG_012262.1:g.92571C=
NG_012262.2:g.92571C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1822C= (TOP1) MANE Select	ENSP00000354522.2:p.Pro608=
ENST00000680945.1:c.415C= (TOP1)	ENSP00000504935.1:p.Pro139=
ENST00000681058.1:n.6608C= (TOP1)
ENST00000681113.1:c.*1517C= (TOP1)	ENSP00000505788.1:n.*1517C=
ENST00000681392.1:n.3130C= (TOP1)
ENST00000681884.1:n.3084C= (TOP1)
ENST00000361337.2:c.1822C= (TOP1)	ENSP00000354522.2:p.Pro608=
NM_003286.2:c.1822C= (TOP1)	NP_003277.1:p.Pro608=
NR_109889.1:n.711-15103G= (PLCG1-AS1)
XM_011529032.1:c.1318C= (TOP1)	XP_011527334.1:p.Pro440=
XM_011529033.1:c.1084C= (TOP1)	XP_011527335.1:p.Pro362=
NM_003286.3:c.1822C= (TOP1)	NP_003277.1:p.Pro608=
NM_003286.4:c.1822C= (TOP1) MANE Select	NP_003277.1:p.Pro608=