Canonical Allele Identifier: CA2410864051
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455138T= , CM000684.2:g.50455138T= GRCh38
NC_000022.10:g.50893567T= , CM000684.1:g.50893567T= GRCh37
NC_000022.9:g.49240433T= NCBI36
NG_041810.1:g.24934A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4481A= ENSP00000252027.8:p.His1494=
ENST00000418590.4:c.191A= ENSP00000401538.2:p.His64=
ENST00000470434.2:n.962A=
ENST00000684986.1:c.4562A= ENSP00000509117.1:p.His1521=
ENST00000685180.1:n.2488+5396A=
ENST00000685390.1:n.2527A=
ENST00000685411.1:n.309A=
ENST00000685592.1:c.793A=
ENST00000685809.1:c.4472A= ENSP00000508863.1:p.His1491=
ENST00000686029.1:c.637A=
ENST00000686191.1:n.3759A=
ENST00000686222.1:c.*3981A= ENSP00000508737.1:n.*3981A=
ENST00000686321.1:c.655A=
ENST00000686427.1:c.*1494A= ENSP00000510379.1:n.*1494A=
ENST00000686758.1:n.2302A=
ENST00000686801.1:c.4547A= ENSP00000509915.1:p.His1516=
ENST00000686826.1:n.878A=
ENST00000687016.1:c.4460A= ENSP00000509074.1:p.His1487=
ENST00000687704.1:c.*2284A= ENSP00000510454.1:n.*2284A=
ENST00000688066.1:c.4559A= ENSP00000510782.1:p.His1520=
ENST00000688124.1:c.*3477A= ENSP00000510645.1:n.*3477A=
ENST00000688848.1:c.*3903A= ENSP00000509419.1:n.*3903A=
ENST00000688985.1:c.1560A= ENSP00000510477.1:n.1560A=
ENST00000689129.1:c.4484A= ENSP00000510414.1:p.His1495=
ENST00000689177.1:n.5831A=
ENST00000689849.1:c.655A=
ENST00000689981.1:c.4559A= ENSP00000509035.1:p.His1520=
ENST00000690369.1:n.4577A=
ENST00000690590.1:n.1606A=
ENST00000690990.1:c.4553A= ENSP00000510461.1:p.His1518=
ENST00000691233.1:c.4478A= ENSP00000509215.1:p.His1493=
ENST00000691306.1:c.657A=
ENST00000691345.1:n.2302+1078A=
ENST00000691792.1:c.4555-8A= ENSP00000509911.1:n.4555-8A=
ENST00000691959.1:n.5278A=
ENST00000692844.1:n.1643A=
ENST00000692946.1:c.655A=
ENST00000693052.1:c.4577A= ENSP00000509558.1:p.His1526=
ENST00000693289.1:n.1718A=
ENST00000693440.1:c.4556A= ENSP00000509462.1:p.His1519=
ENST00000693499.1:n.5484A=
ENST00000693591.1:n.3296A=
ENST00000380817.8:c.4559A= MANE Select ENSP00000370196.2:p.His1520=
ENST00000348911.10:c.4484A= ENSP00000252027.7:p.His1495=
ENST00000380817.7:c.4559A= ENSP00000370196.2:p.His1520=
ENST00000418590.3:c.159A=
ENST00000470434.1:n.700A=
NM_002972.3:c.4559A= NP_002963.2:p.His1520=
XM_005261931.1:c.4562A= XP_005261988.1:p.His1521=
XM_005261935.1:c.4481A= XP_005261992.1:p.His1494=
XM_011530707.1:c.4661A= XP_011529009.1:p.His1554=
XM_011530708.1:c.4613A= XP_011529010.1:p.His1538=
XM_011530709.1:c.4589A= XP_011529011.1:p.His1530=
XM_011530710.1:c.4586A= XP_011529012.1:p.His1529=
XM_011530711.1:c.4586A= XP_011529013.1:p.His1529=
XR_938344.1:n.4679A=
NM_001365819.1:c.4484A= NP_001352748.1:p.His1495=
XM_005261935.2:c.4481A= XP_005261992.1:p.His1494=
XM_011530709.2:c.4589A= XP_011529011.1:p.His1530=
XM_011530710.2:c.4586A= XP_011529012.1:p.His1529=
XM_017028905.2:c.4511A= XP_016884394.1:p.His1504=
NM_002972.4:c.4559A= MANE Select NP_002963.2:p.His1520=