Canonical Allele Identifier: CA2410863999
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455050G= , CM000684.2:g.50455050G= GRCh38
NC_000022.10:g.50893479G= , CM000684.1:g.50893479G= GRCh37
NC_000022.9:g.49240345G= NCBI36
NG_041810.1:g.25022C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4569C= ENSP00000252027.8:p.Phe1523=
ENST00000418590.4:c.279C= ENSP00000401538.2:p.Phe93=
ENST00000470434.2:n.1050C=
ENST00000684986.1:c.4650C= ENSP00000509117.1:p.Phe1550=
ENST00000685180.1:n.2488+5484C=
ENST00000685390.1:n.2615C=
ENST00000685411.1:n.397C=
ENST00000685592.1:c.881C=
ENST00000685809.1:c.4560C= ENSP00000508863.1:p.Phe1520=
ENST00000686029.1:c.725C=
ENST00000686191.1:n.3847C=
ENST00000686222.1:c.*4069C= ENSP00000508737.1:n.*4069C=
ENST00000686321.1:c.743C=
ENST00000686427.1:c.*1582C= ENSP00000510379.1:n.*1582C=
ENST00000686758.1:n.2390C=
ENST00000686801.1:c.4635C= ENSP00000509915.1:p.Phe1545=
ENST00000686826.1:n.966C=
ENST00000687016.1:c.4548C= ENSP00000509074.1:p.Phe1516=
ENST00000687704.1:c.*2372C= ENSP00000510454.1:n.*2372C=
ENST00000688066.1:c.4647C= ENSP00000510782.1:p.Phe1549=
ENST00000688124.1:c.*3565C= ENSP00000510645.1:n.*3565C=
ENST00000688848.1:c.*3991C= ENSP00000509419.1:n.*3991C=
ENST00000688985.1:c.1648C= ENSP00000510477.1:n.1648C=
ENST00000689129.1:c.4572C= ENSP00000510414.1:p.Phe1524=
ENST00000689177.1:n.5919C=
ENST00000689849.1:c.743C=
ENST00000689981.1:c.4647C= ENSP00000509035.1:p.Phe1549=
ENST00000690369.1:n.4665C=
ENST00000690590.1:n.1694C=
ENST00000690990.1:c.4641C= ENSP00000510461.1:p.Phe1547=
ENST00000691233.1:c.4566C= ENSP00000509215.1:p.Phe1522=
ENST00000691306.1:c.745C=
ENST00000691345.1:n.2302+1166C=
ENST00000691792.1:c.4635C= ENSP00000509911.1:p.Phe1545=
ENST00000691959.1:n.5366C=
ENST00000692844.1:n.1731C=
ENST00000692946.1:c.743C=
ENST00000693052.1:c.4665C= ENSP00000509558.1:p.Phe1555=
ENST00000693289.1:n.1806C=
ENST00000693440.1:c.4644C= ENSP00000509462.1:p.Phe1548=
ENST00000693499.1:n.5572C=
ENST00000693591.1:n.3384C=
ENST00000380817.8:c.4647C= MANE Select ENSP00000370196.2:p.Phe1549=
ENST00000348911.10:c.4572C= ENSP00000252027.7:p.Phe1524=
ENST00000380817.7:c.4647C= ENSP00000370196.2:p.Phe1549=
ENST00000418590.3:c.247C=
ENST00000470434.1:n.788C=
NM_002972.3:c.4647C= NP_002963.2:p.Phe1549=
XM_005261931.1:c.4650C= XP_005261988.1:p.Phe1550=
XM_005261935.1:c.4569C= XP_005261992.1:p.Phe1523=
XM_011530707.1:c.4749C= XP_011529009.1:p.Phe1583=
XM_011530708.1:c.4701C= XP_011529010.1:p.Phe1567=
XM_011530709.1:c.4677C= XP_011529011.1:p.Phe1559=
XM_011530710.1:c.4674C= XP_011529012.1:p.Phe1558=
XM_011530711.1:c.4674C= XP_011529013.1:p.Phe1558=
XR_938344.1:n.4767C=
NM_001365819.1:c.4572C= NP_001352748.1:p.Phe1524=
XM_005261935.2:c.4569C= XP_005261992.1:p.Phe1523=
XM_011530709.2:c.4677C= XP_011529011.1:p.Phe1559=
XM_011530710.2:c.4674C= XP_011529012.1:p.Phe1558=
XM_017028905.2:c.4599C= XP_016884394.1:p.Phe1533=
NM_002972.4:c.4647C= MANE Select NP_002963.2:p.Phe1549=