Canonical Allele Identifier: CA2410864031
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455100A= , CM000684.2:g.50455100A= GRCh38
NC_000022.10:g.50893529A= , CM000684.1:g.50893529A= GRCh37
NC_000022.9:g.49240395A= NCBI36
NG_041810.1:g.24972T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4519T= ENSP00000252027.8:p.Tyr1507=
ENST00000418590.4:c.229T= ENSP00000401538.2:p.Tyr77=
ENST00000470434.2:n.1000T=
ENST00000684986.1:c.4600T= ENSP00000509117.1:p.Tyr1534=
ENST00000685180.1:n.2488+5434T=
ENST00000685390.1:n.2565T=
ENST00000685411.1:n.347T=
ENST00000685592.1:c.831T=
ENST00000685809.1:c.4510T= ENSP00000508863.1:p.Tyr1504=
ENST00000686029.1:c.675T=
ENST00000686191.1:n.3797T=
ENST00000686222.1:c.*4019T= ENSP00000508737.1:n.*4019T=
ENST00000686321.1:c.693T=
ENST00000686427.1:c.*1532T= ENSP00000510379.1:n.*1532T=
ENST00000686758.1:n.2340T=
ENST00000686801.1:c.4585T= ENSP00000509915.1:p.Tyr1529=
ENST00000686826.1:n.916T=
ENST00000687016.1:c.4498T= ENSP00000509074.1:p.Tyr1500=
ENST00000687704.1:c.*2322T= ENSP00000510454.1:n.*2322T=
ENST00000688066.1:c.4597T= ENSP00000510782.1:p.Tyr1533=
ENST00000688124.1:c.*3515T= ENSP00000510645.1:n.*3515T=
ENST00000688848.1:c.*3941T= ENSP00000509419.1:n.*3941T=
ENST00000688985.1:c.1598T= ENSP00000510477.1:n.1598T=
ENST00000689129.1:c.4522T= ENSP00000510414.1:p.Tyr1508=
ENST00000689177.1:n.5869T=
ENST00000689849.1:c.693T=
ENST00000689981.1:c.4597T= ENSP00000509035.1:p.Tyr1533=
ENST00000690369.1:n.4615T=
ENST00000690590.1:n.1644T=
ENST00000690990.1:c.4591T= ENSP00000510461.1:p.Tyr1531=
ENST00000691233.1:c.4516T= ENSP00000509215.1:p.Tyr1506=
ENST00000691306.1:c.695T=
ENST00000691345.1:n.2302+1116T=
ENST00000691792.1:c.4585T= ENSP00000509911.1:p.Tyr1529=
ENST00000691959.1:n.5316T=
ENST00000692844.1:n.1681T=
ENST00000692946.1:c.693T=
ENST00000693052.1:c.4615T= ENSP00000509558.1:p.Tyr1539=
ENST00000693289.1:n.1756T=
ENST00000693440.1:c.4594T= ENSP00000509462.1:p.Tyr1532=
ENST00000693499.1:n.5522T=
ENST00000693591.1:n.3334T=
ENST00000380817.8:c.4597T= MANE Select ENSP00000370196.2:p.Tyr1533=
ENST00000348911.10:c.4522T= ENSP00000252027.7:p.Tyr1508=
ENST00000380817.7:c.4597T= ENSP00000370196.2:p.Tyr1533=
ENST00000418590.3:c.197T=
ENST00000470434.1:n.738T=
NM_002972.3:c.4597T= NP_002963.2:p.Tyr1533=
XM_005261931.1:c.4600T= XP_005261988.1:p.Tyr1534=
XM_005261935.1:c.4519T= XP_005261992.1:p.Tyr1507=
XM_011530707.1:c.4699T= XP_011529009.1:p.Tyr1567=
XM_011530708.1:c.4651T= XP_011529010.1:p.Tyr1551=
XM_011530709.1:c.4627T= XP_011529011.1:p.Tyr1543=
XM_011530710.1:c.4624T= XP_011529012.1:p.Tyr1542=
XM_011530711.1:c.4624T= XP_011529013.1:p.Tyr1542=
XR_938344.1:n.4717T=
NM_001365819.1:c.4522T= NP_001352748.1:p.Tyr1508=
XM_005261935.2:c.4519T= XP_005261992.1:p.Tyr1507=
XM_011530709.2:c.4627T= XP_011529011.1:p.Tyr1543=
XM_011530710.2:c.4624T= XP_011529012.1:p.Tyr1542=
XM_017028905.2:c.4549T= XP_016884394.1:p.Tyr1517=
NM_002972.4:c.4597T= MANE Select NP_002963.2:p.Tyr1533=