Canonical Allele Identifier: CA635472943

Gene: TOP1 PLCG1-AS1

Linked Data

• dbSNP Id: rs1416642876
• gnomAD v2: 20-39744571-C-T
• gnomAD v3: 20-41115931-C-T
• gnomAD v4: 20-41115931-C-T
• MyVariant Identifiers: chr20:g.39744571C>T (hg19) ; chr20:g.41115931C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41115931C>T , CM000682.2:g.41115931C>T	GRCh38
NC_000020.10:g.39744571C>T , CM000682.1:g.39744571C>T	GRCh37
NC_000020.9:g.39177985C>T	NCBI36
NG_012262.1:g.92110C>T
NG_012262.2:g.92110C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.1708-347C>T (TOP1) MANE Select	ENSP00000354522.2:n.1708-347C>T
ENST00000680945.1:c.301-347C>T (TOP1)	ENSP00000504935.1:n.301-347C>T
ENST00000681058.1:n.6494-347C>T (TOP1)
ENST00000681113.1:c.*1403-347C>T (TOP1)	ENSP00000505788.1:n.*1403-347C>T
ENST00000681392.1:n.3016-347C>T (TOP1)
ENST00000681884.1:n.2970-347C>T (TOP1)
ENST00000361337.2:c.1708-347C>T (TOP1)	ENSP00000354522.2:n.1708-347C>T
NM_003286.2:c.1708-347C>T (TOP1)	NP_003277.1:n.1708-347C>T
NR_109889.1:n.711-14642G>A (PLCG1-AS1)
XM_011529032.1:c.1204-347C>T (TOP1)	XP_011527334.1:n.1204-347C>T
XM_011529033.1:c.970-347C>T (TOP1)	XP_011527335.1:n.970-347C>T
NM_003286.3:c.1708-347C>T (TOP1)	NP_003277.1:n.1708-347C>T
NM_003286.4:c.1708-347C>T (TOP1) MANE Select	NP_003277.1:n.1708-347C>T