Canonical Allele Identifier: CA409021815

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39744961T>A (hg19) ; chr20:g.41116321T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116321T>A , CM000682.2:g.41116321T>A	GRCh38
NC_000020.10:g.39744961T>A , CM000682.1:g.39744961T>A	GRCh37
NC_000020.9:g.39178375T>A	NCBI36
NG_012262.1:g.92500T>A
NG_012262.2:g.92500T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361337.3:c.1751T>A (TOP1) MANE Select	ENSP00000354522.2:p.Leu584Ter
ENST00000680945.1:c.344T>A (TOP1)	ENSP00000504935.1:p.Leu115Ter
ENST00000681058.1:n.6537T>A (TOP1)
ENST00000681113.1:c.*1446T>A (TOP1)	ENSP00000505788.1:n.*1446T>A
ENST00000681392.1:n.3059T>A (TOP1)
ENST00000681884.1:n.3013T>A (TOP1)
ENST00000361337.2:c.1751T>A (TOP1)	ENSP00000354522.2:p.Leu584Ter
NM_003286.2:c.1751T>A (TOP1)	NP_003277.1:p.Leu584Ter
NR_109889.1:n.711-15032A>T (PLCG1-AS1)
XM_011529032.1:c.1247T>A (TOP1)	XP_011527334.1:p.Leu416Ter
XM_011529033.1:c.1013T>A (TOP1)	XP_011527335.1:p.Leu338Ter
NM_003286.3:c.1751T>A (TOP1)	NP_003277.1:p.Leu584Ter
NM_003286.4:c.1751T>A (TOP1) MANE Select	NP_003277.1:p.Leu584Ter