Canonical Allele Identifier: CA16044420
Gene: SGO2 HGNC NCBI

Linked Data

dbSNP Id: rs1057519602
gnomAD v3: 2-200571795-CAG-C
gnomAD v4: 2-200571795-CAG-C
MyVariant Identifiers: chr2:g.201436522_201436523del (hg19) chr2:g.201436519_201436520del (hg19) chr2:g.200571799_200571800del (hg38) chr2:g.200571796_200571797del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200571799_200571800del , CM000664.2:g.200571799_200571800del GRCh38
NC_000002.11:g.201436522_201436523del , CM000664.1:g.201436522_201436523del GRCh37
NC_000002.10:g.201144767_201144768del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357799.9:c.1453_1454del MANE Select ENSP00000350447.4:p.Glu485LysfsTer5
ENST00000357799.8:c.1453_1454del ENSP00000350447.4:p.Glu485LysfsTer5
NM_001160033.1:c.1453_1454del NP_001153505.1:p.Glu485LysfsTer5
NM_001160046.1:c.1453_1454del NP_001153518.1:p.Glu485LysfsTer5
NM_152524.5:c.1453_1454del NP_689737.4:p.Glu485LysfsTer5
XM_005246344.2:c.1498_1499del XP_005246401.2:p.Glu500LysfsTer5
XM_005246345.2:c.1453_1454del XP_005246402.1:p.Glu485LysfsTer5
XM_011510733.1:c.1453_1454del XP_011509035.1:p.Glu485LysfsTer5
XM_011510734.1:c.1453_1454del XP_011509036.1:p.Glu485LysfsTer5
XM_011510735.1:c.1453_1454del XP_011509037.1:p.Glu485LysfsTer5
XM_005246344.4:c.1498_1499del XP_005246401.2:p.Glu500LysfsTer5
XM_005246345.4:c.1453_1454del XP_005246402.1:p.Glu485LysfsTer5
XM_011510734.3:c.1453_1454del XP_011509036.1:p.Glu485LysfsTer5
XM_017003452.2:c.1543_1544del XP_016858941.1:p.Glu515LysfsTer5
XM_017003453.1:c.1543_1544del XP_016858942.1:p.Glu515LysfsTer5
XM_017003454.2:c.1543_1544del XP_016858943.1:p.Glu515LysfsTer5
NM_152524.6:c.1453_1454del MANE Select NP_689737.4:p.Glu485LysfsTer5
Search 100 bp 5'
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