Canonical Allele Identifier: CA2364230983
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41116513_41116514delinsTC , CM000682.2:g.41116513_41116514delinsTC GRCh38
NC_000020.10:g.39745153_39745154delinsTC , CM000682.1:g.39745153_39745154delinsTC GRCh37
NC_000020.9:g.39178567_39178568delinsTC NCBI36
NG_012262.1:g.92692_92693delinsTC
NG_012262.2:g.92692_92693delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000361337.3:c.1822+121_1822+122delinsTC (TOP1) MANE Select ENSP00000354522.2:n.1822+121_1822+122delinsTC
ENST00000680945.1:c.415+121_415+122delinsTC (TOP1) ENSP00000504935.1:n.415+121_415+122delinsTC
ENST00000681058.1:n.6608+121_6608+122delinsTC (TOP1)
ENST00000681113.1:c.*1517+121_*1517+122delinsTC (TOP1) ENSP00000505788.1:n.*1517+121_*1517+122delinsTC
ENST00000681392.1:n.3130+121_3130+122delinsTC (TOP1)
ENST00000681884.1:n.3084+121_3084+122delinsTC (TOP1)
ENST00000361337.2:c.1822+121_1822+122delinsTC (TOP1) ENSP00000354522.2:n.1822+121_1822+122delinsTC
NM_003286.2:c.1822+121_1822+122delinsTC (TOP1) NP_003277.1:n.1822+121_1822+122delinsTC
NR_109889.1:n.711-15225_711-15224delinsGA (PLCG1-AS1)
XM_011529032.1:c.1318+121_1318+122delinsTC (TOP1) XP_011527334.1:n.1318+121_1318+122delinsTC
XM_011529033.1:c.1084+121_1084+122delinsTC (TOP1) XP_011527335.1:n.1084+121_1084+122delinsTC
NM_003286.3:c.1822+121_1822+122delinsTC (TOP1) NP_003277.1:n.1822+121_1822+122delinsTC
NM_003286.4:c.1822+121_1822+122delinsTC (TOP1) MANE Select NP_003277.1:n.1822+121_1822+122delinsTC