Canonical Allele Identifier: CA2410863932
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50454934A= , CM000684.2:g.50454934A= GRCh38
NC_000022.10:g.50893363A= , CM000684.1:g.50893363A= GRCh37
NC_000022.9:g.49240229A= NCBI36
NG_041810.1:g.25138T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4614T= ENSP00000252027.8:p.Tyr1538=
ENST00000418590.4:c.324T= ENSP00000401538.2:p.Tyr108=
ENST00000470434.2:n.1095T=
ENST00000684986.1:c.4695T= ENSP00000509117.1:p.Tyr1565=
ENST00000685180.1:n.2488+5600T=
ENST00000685390.1:n.2660T=
ENST00000685411.1:n.442T=
ENST00000685592.1:c.926T=
ENST00000685809.1:c.4605T= ENSP00000508863.1:p.Tyr1535=
ENST00000686029.1:c.770T=
ENST00000686191.1:n.3892T=
ENST00000686222.1:c.*4114T= ENSP00000508737.1:n.*4114T=
ENST00000686321.1:c.788T=
ENST00000686427.1:c.*1627T= ENSP00000510379.1:n.*1627T=
ENST00000686758.1:n.2506T=
ENST00000686801.1:c.4680T= ENSP00000509915.1:p.Tyr1560=
ENST00000686826.1:n.1011T=
ENST00000687016.1:c.4593T= ENSP00000509074.1:p.Tyr1531=
ENST00000687704.1:c.*2417T= ENSP00000510454.1:n.*2417T=
ENST00000688066.1:c.4692T= ENSP00000510782.1:p.Tyr1564=
ENST00000688124.1:c.*3610T= ENSP00000510645.1:n.*3610T=
ENST00000688848.1:c.*4036T= ENSP00000509419.1:n.*4036T=
ENST00000688985.1:c.1693T= ENSP00000510477.1:n.1693T=
ENST00000689129.1:c.4617T= ENSP00000510414.1:p.Tyr1539=
ENST00000689177.1:n.5964T=
ENST00000689849.1:c.788T=
ENST00000689981.1:c.4692T= ENSP00000509035.1:p.Tyr1564=
ENST00000690369.1:n.4710T=
ENST00000690590.1:n.1739T=
ENST00000690990.1:c.4686T= ENSP00000510461.1:p.Tyr1562=
ENST00000691233.1:c.4611T= ENSP00000509215.1:p.Tyr1537=
ENST00000691306.1:c.780-7T=
ENST00000691345.1:n.2302+1282T=
ENST00000691792.1:c.4680T= ENSP00000509911.1:p.Tyr1560=
ENST00000691959.1:n.5411T=
ENST00000692844.1:n.1776T=
ENST00000692946.1:c.788T=
ENST00000693052.1:c.4710T= ENSP00000509558.1:p.Tyr1570=
ENST00000693289.1:n.1851T=
ENST00000693440.1:c.4689T= ENSP00000509462.1:p.Tyr1563=
ENST00000693499.1:n.5688T=
ENST00000693591.1:n.3500T=
ENST00000380817.8:c.4692T= MANE Select ENSP00000370196.2:p.Tyr1564=
ENST00000348911.10:c.4617T= ENSP00000252027.7:p.Tyr1539=
ENST00000380817.7:c.4692T= ENSP00000370196.2:p.Tyr1564=
ENST00000418590.3:c.292T=
ENST00000470434.1:n.833T=
NM_002972.3:c.4692T= NP_002963.2:p.Tyr1564=
XM_005261931.1:c.4695T= XP_005261988.1:p.Tyr1565=
XM_005261935.1:c.4614T= XP_005261992.1:p.Tyr1538=
XM_011530707.1:c.4794T= XP_011529009.1:p.Tyr1598=
XM_011530708.1:c.4746T= XP_011529010.1:p.Tyr1582=
XM_011530709.1:c.4722T= XP_011529011.1:p.Tyr1574=
XM_011530710.1:c.4719T= XP_011529012.1:p.Tyr1573=
XM_011530711.1:c.4719T= XP_011529013.1:p.Tyr1573=
XR_938344.1:n.4812T=
NM_001365819.1:c.4617T= NP_001352748.1:p.Tyr1539=
XM_005261935.2:c.4614T= XP_005261992.1:p.Tyr1538=
XM_011530709.2:c.4722T= XP_011529011.1:p.Tyr1574=
XM_011530710.2:c.4719T= XP_011529012.1:p.Tyr1573=
XM_017028905.2:c.4644T= XP_016884394.1:p.Tyr1548=
NM_002972.4:c.4692T= MANE Select NP_002963.2:p.Tyr1564=