Canonical Allele Identifier: CA510555100

Gene: TOP1 PLCG1-AS1

Linked Data

• MyVariant Identifiers: chr20:g.39745001G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41116361G>C , CM000682.2:g.41116361G>C	GRCh38
NC_000020.10:g.39745001G>C , CM000682.1:g.39745001G>C	GRCh37
NC_000020.9:g.39178415G>C	NCBI36
NG_012262.1:g.92540G>C
NG_012262.2:g.92540G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1791G>C (TOP1) MANE Select	ENSP00000354522.2:p.Thr597=
ENST00000680945.1:c.384G>C (TOP1)	ENSP00000504935.1:p.Thr128=
ENST00000681058.1:n.6577G>C (TOP1)
ENST00000681113.1:c.*1486G>C (TOP1)	ENSP00000505788.1:n.*1486G>C
ENST00000681392.1:n.3099G>C (TOP1)
ENST00000681884.1:n.3053G>C (TOP1)
ENST00000361337.2:c.1791G>C (TOP1)	ENSP00000354522.2:p.Thr597=
NM_003286.2:c.1791G>C (TOP1)	NP_003277.1:p.Thr597=
NR_109889.1:n.711-15072C>G (PLCG1-AS1)
XM_011529032.1:c.1287G>C (TOP1)	XP_011527334.1:p.Thr429=
XM_011529033.1:c.1053G>C (TOP1)	XP_011527335.1:p.Thr351=
NM_003286.3:c.1791G>C (TOP1)	NP_003277.1:p.Thr597=
NM_003286.4:c.1791G>C (TOP1) MANE Select	NP_003277.1:p.Thr597=