Canonical Allele Identifier: CA2364230889
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2034328087

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41116240_41116245dup , CM000682.2:g.41116240_41116245dup GRCh38
NC_000020.10:g.39744880_39744885dup , CM000682.1:g.39744880_39744885dup GRCh37
NC_000020.9:g.39178294_39178299dup NCBI36
NG_012262.1:g.92419_92424dup
NG_012262.2:g.92419_92424dup

Transcript Alleles

HGVS Amino-acid change
ENST00000361337.3:c.1708-38_1708-33dup (TOP1) MANE Select ENSP00000354522.2:n.1708-38_1708-33dup
ENST00000680945.1:c.301-38_301-33dup (TOP1) ENSP00000504935.1:n.301-38_301-33dup
ENST00000681058.1:n.6494-38_6494-33dup (TOP1)
ENST00000681113.1:c.*1403-38_*1403-33dup (TOP1) ENSP00000505788.1:n.*1403-38_*1403-33dup
ENST00000681392.1:n.3016-38_3016-33dup (TOP1)
ENST00000681884.1:n.2970-38_2970-33dup (TOP1)
ENST00000361337.2:c.1708-38_1708-33dup (TOP1) ENSP00000354522.2:n.1708-38_1708-33dup
NM_003286.2:c.1708-38_1708-33dup (TOP1) NP_003277.1:n.1708-38_1708-33dup
NR_109889.1:n.711-14955_711-14950dup (PLCG1-AS1)
XM_011529032.1:c.1204-38_1204-33dup (TOP1) XP_011527334.1:n.1204-38_1204-33dup
XM_011529033.1:c.970-38_970-33dup (TOP1) XP_011527335.1:n.970-38_970-33dup
NM_003286.3:c.1708-38_1708-33dup (TOP1) NP_003277.1:n.1708-38_1708-33dup
NM_003286.4:c.1708-38_1708-33dup (TOP1) MANE Select NP_003277.1:n.1708-38_1708-33dup