Canonical Allele Identifier: CA2364230931
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41116417_41116420delinsGCCC , CM000682.2:g.41116417_41116420delinsGCCC GRCh38
NC_000020.10:g.39745057_39745060delinsGCCC , CM000682.1:g.39745057_39745060delinsGCCC GRCh37
NC_000020.9:g.39178471_39178474delinsGCCC NCBI36
NG_012262.1:g.92596_92599delinsGCCC
NG_012262.2:g.92596_92599delinsGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000361337.3:c.1822+25_1822+28delinsGCCC (TOP1) MANE Select ENSP00000354522.2:n.1822+25_1822+28delinsGCCC
ENST00000680945.1:c.415+25_415+28delinsGCCC (TOP1) ENSP00000504935.1:n.415+25_415+28delinsGCCC
ENST00000681058.1:n.6608+25_6608+28delinsGCCC (TOP1)
ENST00000681113.1:c.*1517+25_*1517+28delinsGCCC (TOP1) ENSP00000505788.1:n.*1517+25_*1517+28delinsGCCC
ENST00000681392.1:n.3130+25_3130+28delinsGCCC (TOP1)
ENST00000681884.1:n.3084+25_3084+28delinsGCCC (TOP1)
ENST00000361337.2:c.1822+25_1822+28delinsGCCC (TOP1) ENSP00000354522.2:n.1822+25_1822+28delinsGCCC
NM_003286.2:c.1822+25_1822+28delinsGCCC (TOP1) NP_003277.1:n.1822+25_1822+28delinsGCCC
NR_109889.1:n.711-15131_711-15128delinsGGGC (PLCG1-AS1)
XM_011529032.1:c.1318+25_1318+28delinsGCCC (TOP1) XP_011527334.1:n.1318+25_1318+28delinsGCCC
XM_011529033.1:c.1084+25_1084+28delinsGCCC (TOP1) XP_011527335.1:n.1084+25_1084+28delinsGCCC
NM_003286.3:c.1822+25_1822+28delinsGCCC (TOP1) NP_003277.1:n.1822+25_1822+28delinsGCCC
NM_003286.4:c.1822+25_1822+28delinsGCCC (TOP1) MANE Select NP_003277.1:n.1822+25_1822+28delinsGCCC