Canonical Allele Identifier: CA2410864038
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455118A= , CM000684.2:g.50455118A= GRCh38
NC_000022.10:g.50893547A= , CM000684.1:g.50893547A= GRCh37
NC_000022.9:g.49240413A= NCBI36
NG_041810.1:g.24954T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4501T= ENSP00000252027.8:p.Phe1501=
ENST00000418590.4:c.211T= ENSP00000401538.2:p.Phe71=
ENST00000470434.2:n.982T=
ENST00000684986.1:c.4582T= ENSP00000509117.1:p.Phe1528=
ENST00000685180.1:n.2488+5416T=
ENST00000685390.1:n.2547T=
ENST00000685411.1:n.329T=
ENST00000685592.1:c.813T=
ENST00000685809.1:c.4492T= ENSP00000508863.1:p.Phe1498=
ENST00000686029.1:c.657T=
ENST00000686191.1:n.3779T=
ENST00000686222.1:c.*4001T= ENSP00000508737.1:n.*4001T=
ENST00000686321.1:c.675T=
ENST00000686427.1:c.*1514T= ENSP00000510379.1:n.*1514T=
ENST00000686758.1:n.2322T=
ENST00000686801.1:c.4567T= ENSP00000509915.1:p.Phe1523=
ENST00000686826.1:n.898T=
ENST00000687016.1:c.4480T= ENSP00000509074.1:p.Phe1494=
ENST00000687704.1:c.*2304T= ENSP00000510454.1:n.*2304T=
ENST00000688066.1:c.4579T= ENSP00000510782.1:p.Phe1527=
ENST00000688124.1:c.*3497T= ENSP00000510645.1:n.*3497T=
ENST00000688848.1:c.*3923T= ENSP00000509419.1:n.*3923T=
ENST00000688985.1:c.1580T= ENSP00000510477.1:n.1580T=
ENST00000689129.1:c.4504T= ENSP00000510414.1:p.Phe1502=
ENST00000689177.1:n.5851T=
ENST00000689849.1:c.675T=
ENST00000689981.1:c.4579T= ENSP00000509035.1:p.Phe1527=
ENST00000690369.1:n.4597T=
ENST00000690590.1:n.1626T=
ENST00000690990.1:c.4573T= ENSP00000510461.1:p.Phe1525=
ENST00000691233.1:c.4498T= ENSP00000509215.1:p.Phe1500=
ENST00000691306.1:c.677T=
ENST00000691345.1:n.2302+1098T=
ENST00000691792.1:c.4567T= ENSP00000509911.1:p.Phe1523=
ENST00000691959.1:n.5298T=
ENST00000692844.1:n.1663T=
ENST00000692946.1:c.675T=
ENST00000693052.1:c.4597T= ENSP00000509558.1:p.Phe1533=
ENST00000693289.1:n.1738T=
ENST00000693440.1:c.4576T= ENSP00000509462.1:p.Phe1526=
ENST00000693499.1:n.5504T=
ENST00000693591.1:n.3316T=
ENST00000380817.8:c.4579T= MANE Select ENSP00000370196.2:p.Phe1527=
ENST00000348911.10:c.4504T= ENSP00000252027.7:p.Phe1502=
ENST00000380817.7:c.4579T= ENSP00000370196.2:p.Phe1527=
ENST00000418590.3:c.179T=
ENST00000470434.1:n.720T=
NM_002972.3:c.4579T= NP_002963.2:p.Phe1527=
XM_005261931.1:c.4582T= XP_005261988.1:p.Phe1528=
XM_005261935.1:c.4501T= XP_005261992.1:p.Phe1501=
XM_011530707.1:c.4681T= XP_011529009.1:p.Phe1561=
XM_011530708.1:c.4633T= XP_011529010.1:p.Phe1545=
XM_011530709.1:c.4609T= XP_011529011.1:p.Phe1537=
XM_011530710.1:c.4606T= XP_011529012.1:p.Phe1536=
XM_011530711.1:c.4606T= XP_011529013.1:p.Phe1536=
XR_938344.1:n.4699T=
NM_001365819.1:c.4504T= NP_001352748.1:p.Phe1502=
XM_005261935.2:c.4501T= XP_005261992.1:p.Phe1501=
XM_011530709.2:c.4609T= XP_011529011.1:p.Phe1537=
XM_011530710.2:c.4606T= XP_011529012.1:p.Phe1536=
XM_017028905.2:c.4531T= XP_016884394.1:p.Phe1511=
NM_002972.4:c.4579T= MANE Select NP_002963.2:p.Phe1527=