Canonical Allele Identifier: CA2410863901
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50454887C= , CM000684.2:g.50454887C= GRCh38
NC_000022.10:g.50893316C= , CM000684.1:g.50893316C= GRCh37
NC_000022.9:g.49240182C= NCBI36
NG_041810.1:g.25185G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4661G= ENSP00000252027.8:p.Trp1554=
ENST00000418590.4:c.371G= ENSP00000401538.2:p.Trp124=
ENST00000470434.2:n.1142G=
ENST00000684986.1:c.4742G= ENSP00000509117.1:p.Trp1581=
ENST00000685180.1:n.2488+5647G=
ENST00000685390.1:n.2707G=
ENST00000685411.1:n.489G=
ENST00000685592.1:c.973G=
ENST00000685809.1:c.4652G= ENSP00000508863.1:p.Trp1551=
ENST00000686029.1:c.817G=
ENST00000686191.1:n.3939G=
ENST00000686222.1:c.*4161G= ENSP00000508737.1:n.*4161G=
ENST00000686321.1:c.835G=
ENST00000686427.1:c.*1674G= ENSP00000510379.1:n.*1674G=
ENST00000686758.1:n.2553G=
ENST00000686801.1:c.4727G= ENSP00000509915.1:p.Trp1576=
ENST00000686826.1:n.1058G=
ENST00000687016.1:c.4640G= ENSP00000509074.1:p.Trp1547=
ENST00000687704.1:c.*2464G= ENSP00000510454.1:n.*2464G=
ENST00000688066.1:c.4739G= ENSP00000510782.1:p.Trp1580=
ENST00000688124.1:c.*3657G= ENSP00000510645.1:n.*3657G=
ENST00000688848.1:c.*4083G= ENSP00000509419.1:n.*4083G=
ENST00000688985.1:c.1740G= ENSP00000510477.1:n.1740G=
ENST00000689129.1:c.4664G= ENSP00000510414.1:p.Trp1555=
ENST00000689177.1:n.6011G=
ENST00000689849.1:c.835G=
ENST00000689981.1:c.4739G= ENSP00000509035.1:p.Trp1580=
ENST00000690369.1:n.4757G=
ENST00000690590.1:n.1786G=
ENST00000690990.1:c.4733G= ENSP00000510461.1:p.Trp1578=
ENST00000691233.1:c.4658G= ENSP00000509215.1:p.Trp1553=
ENST00000691306.1:c.820G=
ENST00000691345.1:n.2302+1329G=
ENST00000691792.1:c.4727G= ENSP00000509911.1:p.Trp1576=
ENST00000691959.1:n.5458G=
ENST00000692844.1:n.1823G=
ENST00000692946.1:c.835G=
ENST00000693052.1:c.4757G= ENSP00000509558.1:p.Trp1586=
ENST00000693289.1:n.1898G=
ENST00000693440.1:c.4736G= ENSP00000509462.1:p.Trp1579=
ENST00000693499.1:n.5735G=
ENST00000693591.1:n.3547G=
ENST00000380817.8:c.4739G= MANE Select ENSP00000370196.2:p.Trp1580=
ENST00000348911.10:c.4664G= ENSP00000252027.7:p.Trp1555=
ENST00000380817.7:c.4739G= ENSP00000370196.2:p.Trp1580=
ENST00000418590.3:c.339G=
ENST00000470434.1:n.880G=
NM_002972.3:c.4739G= NP_002963.2:p.Trp1580=
XM_005261931.1:c.4742G= XP_005261988.1:p.Trp1581=
XM_005261935.1:c.4661G= XP_005261992.1:p.Trp1554=
XM_011530707.1:c.4841G= XP_011529009.1:p.Trp1614=
XM_011530708.1:c.4793G= XP_011529010.1:p.Trp1598=
XM_011530709.1:c.4769G= XP_011529011.1:p.Trp1590=
XM_011530710.1:c.4766G= XP_011529012.1:p.Trp1589=
XM_011530711.1:c.4766G= XP_011529013.1:p.Trp1589=
XR_938344.1:n.4859G=
NM_001365819.1:c.4664G= NP_001352748.1:p.Trp1555=
XM_005261935.2:c.4661G= XP_005261992.1:p.Trp1554=
XM_011530709.2:c.4769G= XP_011529011.1:p.Trp1590=
XM_011530710.2:c.4766G= XP_011529012.1:p.Trp1589=
XM_017028905.2:c.4691G= XP_016884394.1:p.Trp1564=
NM_002972.4:c.4739G= MANE Select NP_002963.2:p.Trp1580=