Canonical Allele Identifier: CA409021839
Gene: TOP1 HGNC NCBI
PLCG1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.41116331G>T , CM000682.2:g.41116331G>T GRCh38
NC_000020.10:g.39744971G>T , CM000682.1:g.39744971G>T GRCh37
NC_000020.9:g.39178385G>T NCBI36
NG_012262.1:g.92510G>T
NG_012262.2:g.92510G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361337.3:c.1761G>T (TOP1) MANE Select ENSP00000354522.2:p.Lys587Asn
ENST00000680945.1:c.354G>T (TOP1) ENSP00000504935.1:p.Lys118Asn
ENST00000681058.1:n.6547G>T (TOP1)
ENST00000681113.1:c.*1456G>T (TOP1) ENSP00000505788.1:n.*1456G>T
ENST00000681392.1:n.3069G>T (TOP1)
ENST00000681884.1:n.3023G>T (TOP1)
ENST00000361337.2:c.1761G>T (TOP1) ENSP00000354522.2:p.Lys587Asn
NM_003286.2:c.1761G>T (TOP1) NP_003277.1:p.Lys587Asn
NR_109889.1:n.711-15042C>A (PLCG1-AS1)
XM_011529032.1:c.1257G>T (TOP1) XP_011527334.1:p.Lys419Asn
XM_011529033.1:c.1023G>T (TOP1) XP_011527335.1:p.Lys341Asn
NM_003286.3:c.1761G>T (TOP1) NP_003277.1:p.Lys587Asn
NM_003286.4:c.1761G>T (TOP1) MANE Select NP_003277.1:p.Lys587Asn