Canonical Allele Identifier: CA409021903

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744999A>T (hg19) ; chr20:g.41116359A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116359A>T , CM000682.2:g.41116359A>T	GRCh38
NC_000020.10:g.39744999A>T , CM000682.1:g.39744999A>T	GRCh37
NC_000020.9:g.39178413A>T	NCBI36
NG_012262.1:g.92538A>T
NG_012262.2:g.92538A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1789A>T (TOP1) MANE Select	ENSP00000354522.2:p.Thr597Ser
ENST00000680945.1:c.382A>T (TOP1)	ENSP00000504935.1:p.Thr128Ser
ENST00000681058.1:n.6575A>T (TOP1)
ENST00000681113.1:c.*1484A>T (TOP1)	ENSP00000505788.1:n.*1484A>T
ENST00000681392.1:n.3097A>T (TOP1)
ENST00000681884.1:n.3051A>T (TOP1)
ENST00000361337.2:c.1789A>T (TOP1)	ENSP00000354522.2:p.Thr597Ser
NM_003286.2:c.1789A>T (TOP1)	NP_003277.1:p.Thr597Ser
NR_109889.1:n.711-15070T>A (PLCG1-AS1)
XM_011529032.1:c.1285A>T (TOP1)	XP_011527334.1:p.Thr429Ser
XM_011529033.1:c.1051A>T (TOP1)	XP_011527335.1:p.Thr351Ser
NM_003286.3:c.1789A>T (TOP1)	NP_003277.1:p.Thr597Ser
NM_003286.4:c.1789A>T (TOP1) MANE Select	NP_003277.1:p.Thr597Ser