Canonical Allele Identifier: CA409021744

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744931A>T (hg19) ; chr20:g.41116291A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116291A>T , CM000682.2:g.41116291A>T	GRCh38
NC_000020.10:g.39744931A>T , CM000682.1:g.39744931A>T	GRCh37
NC_000020.9:g.39178345A>T	NCBI36
NG_012262.1:g.92470A>T
NG_012262.2:g.92470A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1721A>T (TOP1) MANE Select	ENSP00000354522.2:p.Asn574Ile
ENST00000680945.1:c.314A>T (TOP1)	ENSP00000504935.1:p.Asn105Ile
ENST00000681058.1:n.6507A>T (TOP1)
ENST00000681113.1:c.*1416A>T (TOP1)	ENSP00000505788.1:n.*1416A>T
ENST00000681392.1:n.3029A>T (TOP1)
ENST00000681884.1:n.2983A>T (TOP1)
ENST00000361337.2:c.1721A>T (TOP1)	ENSP00000354522.2:p.Asn574Ile
NM_003286.2:c.1721A>T (TOP1)	NP_003277.1:p.Asn574Ile
NR_109889.1:n.711-15002T>A (PLCG1-AS1)
XM_011529032.1:c.1217A>T (TOP1)	XP_011527334.1:p.Asn406Ile
XM_011529033.1:c.983A>T (TOP1)	XP_011527335.1:p.Asn328Ile
NM_003286.3:c.1721A>T (TOP1)	NP_003277.1:p.Asn574Ile
NM_003286.4:c.1721A>T (TOP1) MANE Select	NP_003277.1:p.Asn574Ile