Canonical Allele Identifier: CA2410864037
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455115C= , CM000684.2:g.50455115C= GRCh38
NC_000022.10:g.50893544C= , CM000684.1:g.50893544C= GRCh37
NC_000022.9:g.49240410C= NCBI36
NG_041810.1:g.24957G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4504G= ENSP00000252027.8:p.Glu1502=
ENST00000418590.4:c.214G= ENSP00000401538.2:p.Glu72=
ENST00000470434.2:n.985G=
ENST00000684986.1:c.4585G= ENSP00000509117.1:p.Glu1529=
ENST00000685180.1:n.2488+5419G=
ENST00000685390.1:n.2550G=
ENST00000685411.1:n.332G=
ENST00000685592.1:c.816G=
ENST00000685809.1:c.4495G= ENSP00000508863.1:p.Glu1499=
ENST00000686029.1:c.660G=
ENST00000686191.1:n.3782G=
ENST00000686222.1:c.*4004G= ENSP00000508737.1:n.*4004G=
ENST00000686321.1:c.678G=
ENST00000686427.1:c.*1517G= ENSP00000510379.1:n.*1517G=
ENST00000686758.1:n.2325G=
ENST00000686801.1:c.4570G= ENSP00000509915.1:p.Glu1524=
ENST00000686826.1:n.901G=
ENST00000687016.1:c.4483G= ENSP00000509074.1:p.Glu1495=
ENST00000687704.1:c.*2307G= ENSP00000510454.1:n.*2307G=
ENST00000688066.1:c.4582G= ENSP00000510782.1:p.Glu1528=
ENST00000688124.1:c.*3500G= ENSP00000510645.1:n.*3500G=
ENST00000688848.1:c.*3926G= ENSP00000509419.1:n.*3926G=
ENST00000688985.1:c.1583G= ENSP00000510477.1:n.1583G=
ENST00000689129.1:c.4507G= ENSP00000510414.1:p.Glu1503=
ENST00000689177.1:n.5854G=
ENST00000689849.1:c.678G=
ENST00000689981.1:c.4582G= ENSP00000509035.1:p.Glu1528=
ENST00000690369.1:n.4600G=
ENST00000690590.1:n.1629G=
ENST00000690990.1:c.4576G= ENSP00000510461.1:p.Glu1526=
ENST00000691233.1:c.4501G= ENSP00000509215.1:p.Glu1501=
ENST00000691306.1:c.680G=
ENST00000691345.1:n.2302+1101G=
ENST00000691792.1:c.4570G= ENSP00000509911.1:p.Glu1524=
ENST00000691959.1:n.5301G=
ENST00000692844.1:n.1666G=
ENST00000692946.1:c.678G=
ENST00000693052.1:c.4600G= ENSP00000509558.1:p.Glu1534=
ENST00000693289.1:n.1741G=
ENST00000693440.1:c.4579G= ENSP00000509462.1:p.Glu1527=
ENST00000693499.1:n.5507G=
ENST00000693591.1:n.3319G=
ENST00000380817.8:c.4582G= MANE Select ENSP00000370196.2:p.Glu1528=
ENST00000348911.10:c.4507G= ENSP00000252027.7:p.Glu1503=
ENST00000380817.7:c.4582G= ENSP00000370196.2:p.Glu1528=
ENST00000418590.3:c.182G=
ENST00000470434.1:n.723G=
NM_002972.3:c.4582G= NP_002963.2:p.Glu1528=
XM_005261931.1:c.4585G= XP_005261988.1:p.Glu1529=
XM_005261935.1:c.4504G= XP_005261992.1:p.Glu1502=
XM_011530707.1:c.4684G= XP_011529009.1:p.Glu1562=
XM_011530708.1:c.4636G= XP_011529010.1:p.Glu1546=
XM_011530709.1:c.4612G= XP_011529011.1:p.Glu1538=
XM_011530710.1:c.4609G= XP_011529012.1:p.Glu1537=
XM_011530711.1:c.4609G= XP_011529013.1:p.Glu1537=
XR_938344.1:n.4702G=
NM_001365819.1:c.4507G= NP_001352748.1:p.Glu1503=
XM_005261935.2:c.4504G= XP_005261992.1:p.Glu1502=
XM_011530709.2:c.4612G= XP_011529011.1:p.Glu1538=
XM_011530710.2:c.4609G= XP_011529012.1:p.Glu1537=
XM_017028905.2:c.4534G= XP_016884394.1:p.Glu1512=
NM_002972.4:c.4582G= MANE Select NP_002963.2:p.Glu1528=