Canonical Allele Identifier: CA2410864005
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455064G= , CM000684.2:g.50455064G= GRCh38
NC_000022.10:g.50893493G= , CM000684.1:g.50893493G= GRCh37
NC_000022.9:g.49240359G= NCBI36
NG_041810.1:g.25008C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4555C= ENSP00000252027.8:p.Arg1519=
ENST00000418590.4:c.265C= ENSP00000401538.2:p.Arg89=
ENST00000470434.2:n.1036C=
ENST00000684986.1:c.4636C= ENSP00000509117.1:p.Arg1546=
ENST00000685180.1:n.2488+5470C=
ENST00000685390.1:n.2601C=
ENST00000685411.1:n.383C=
ENST00000685592.1:c.867C=
ENST00000685809.1:c.4546C= ENSP00000508863.1:p.Arg1516=
ENST00000686029.1:c.711C=
ENST00000686191.1:n.3833C=
ENST00000686222.1:c.*4055C= ENSP00000508737.1:n.*4055C=
ENST00000686321.1:c.729C=
ENST00000686427.1:c.*1568C= ENSP00000510379.1:n.*1568C=
ENST00000686758.1:n.2376C=
ENST00000686801.1:c.4621C= ENSP00000509915.1:p.Arg1541=
ENST00000686826.1:n.952C=
ENST00000687016.1:c.4534C= ENSP00000509074.1:p.Arg1512=
ENST00000687704.1:c.*2358C= ENSP00000510454.1:n.*2358C=
ENST00000688066.1:c.4633C= ENSP00000510782.1:p.Arg1545=
ENST00000688124.1:c.*3551C= ENSP00000510645.1:n.*3551C=
ENST00000688848.1:c.*3977C= ENSP00000509419.1:n.*3977C=
ENST00000688985.1:c.1634C= ENSP00000510477.1:n.1634C=
ENST00000689129.1:c.4558C= ENSP00000510414.1:p.Arg1520=
ENST00000689177.1:n.5905C=
ENST00000689849.1:c.729C=
ENST00000689981.1:c.4633C= ENSP00000509035.1:p.Arg1545=
ENST00000690369.1:n.4651C=
ENST00000690590.1:n.1680C=
ENST00000690990.1:c.4627C= ENSP00000510461.1:p.Arg1543=
ENST00000691233.1:c.4552C= ENSP00000509215.1:p.Arg1518=
ENST00000691306.1:c.731C=
ENST00000691345.1:n.2302+1152C=
ENST00000691792.1:c.4621C= ENSP00000509911.1:p.Arg1541=
ENST00000691959.1:n.5352C=
ENST00000692844.1:n.1717C=
ENST00000692946.1:c.729C=
ENST00000693052.1:c.4651C= ENSP00000509558.1:p.Arg1551=
ENST00000693289.1:n.1792C=
ENST00000693440.1:c.4630C= ENSP00000509462.1:p.Arg1544=
ENST00000693499.1:n.5558C=
ENST00000693591.1:n.3370C=
ENST00000380817.8:c.4633C= MANE Select ENSP00000370196.2:p.Arg1545=
ENST00000348911.10:c.4558C= ENSP00000252027.7:p.Arg1520=
ENST00000380817.7:c.4633C= ENSP00000370196.2:p.Arg1545=
ENST00000418590.3:c.233C=
ENST00000470434.1:n.774C=
NM_002972.3:c.4633C= NP_002963.2:p.Arg1545=
XM_005261931.1:c.4636C= XP_005261988.1:p.Arg1546=
XM_005261935.1:c.4555C= XP_005261992.1:p.Arg1519=
XM_011530707.1:c.4735C= XP_011529009.1:p.Arg1579=
XM_011530708.1:c.4687C= XP_011529010.1:p.Arg1563=
XM_011530709.1:c.4663C= XP_011529011.1:p.Arg1555=
XM_011530710.1:c.4660C= XP_011529012.1:p.Arg1554=
XM_011530711.1:c.4660C= XP_011529013.1:p.Arg1554=
XR_938344.1:n.4753C=
NM_001365819.1:c.4558C= NP_001352748.1:p.Arg1520=
XM_005261935.2:c.4555C= XP_005261992.1:p.Arg1519=
XM_011530709.2:c.4663C= XP_011529011.1:p.Arg1555=
XM_011530710.2:c.4660C= XP_011529012.1:p.Arg1554=
XM_017028905.2:c.4585C= XP_016884394.1:p.Arg1529=
NM_002972.4:c.4633C= MANE Select NP_002963.2:p.Arg1545=