Canonical Allele Identifier: CA2364230738
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41115933_41115945delinsAGGTGTGGTAGTC , CM000682.2:g.41115933_41115945delinsAGGTGTGGTAGTC GRCh38
NC_000020.10:g.39744573_39744585delinsAGGTGTGGTAGTC , CM000682.1:g.39744573_39744585delinsAGGTGTGGTAGTC GRCh37
NC_000020.9:g.39177987_39177999delinsAGGTGTGGTAGTC NCBI36
NG_012262.1:g.92112_92124delinsAGGTGTGGTAGTC
NG_012262.2:g.92112_92124delinsAGGTGTGGTAGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000361337.3:c.1708-345_1708-333delinsAGGTGTGGTAGTC (TOP1) MANE Select ENSP00000354522.2:n.1708-345_1708-333delinsAGGTGTGGTAGTC
ENST00000680945.1:c.301-345_301-333delinsAGGTGTGGTAGTC (TOP1) ENSP00000504935.1:n.301-345_301-333delinsAGGTGTGGTAGTC
ENST00000681058.1:n.6494-345_6494-333delinsAGGTGTGGTAGTC (TOP1)
ENST00000681113.1:c.*1403-345_*1403-333delinsAGGTGTGGTAGTC (TOP1) ENSP00000505788.1:n.*1403-345_*1403-333delinsAGGTGTGGTAGTC
ENST00000681392.1:n.3016-345_3016-333delinsAGGTGTGGTAGTC (TOP1)
ENST00000681884.1:n.2970-345_2970-333delinsAGGTGTGGTAGTC (TOP1)
ENST00000361337.2:c.1708-345_1708-333delinsAGGTGTGGTAGTC (TOP1) ENSP00000354522.2:n.1708-345_1708-333delinsAGGTGTGGTAGTC
NM_003286.2:c.1708-345_1708-333delinsAGGTGTGGTAGTC (TOP1) NP_003277.1:n.1708-345_1708-333delinsAGGTGTGGTAGTC
NR_109889.1:n.711-14656_711-14644delinsGACTACCACACCT (PLCG1-AS1)
XM_011529032.1:c.1204-345_1204-333delinsAGGTGTGGTAGTC (TOP1) XP_011527334.1:n.1204-345_1204-333delinsAGGTGTGGTAGTC
XM_011529033.1:c.970-345_970-333delinsAGGTGTGGTAGTC (TOP1) XP_011527335.1:n.970-345_970-333delinsAGGTGTGGTAGTC
NM_003286.3:c.1708-345_1708-333delinsAGGTGTGGTAGTC (TOP1) NP_003277.1:n.1708-345_1708-333delinsAGGTGTGGTAGTC
NM_003286.4:c.1708-345_1708-333delinsAGGTGTGGTAGTC (TOP1) MANE Select NP_003277.1:n.1708-345_1708-333delinsAGGTGTGGTAGTC