Canonical Allele Identifier: CA2410864032
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455105T= , CM000684.2:g.50455105T= GRCh38
NC_000022.10:g.50893534T= , CM000684.1:g.50893534T= GRCh37
NC_000022.9:g.49240400T= NCBI36
NG_041810.1:g.24967A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4514A= ENSP00000252027.8:p.Gln1505=
ENST00000418590.4:c.224A= ENSP00000401538.2:p.Gln75=
ENST00000470434.2:n.995A=
ENST00000684986.1:c.4595A= ENSP00000509117.1:p.Gln1532=
ENST00000685180.1:n.2488+5429A=
ENST00000685390.1:n.2560A=
ENST00000685411.1:n.342A=
ENST00000685592.1:c.826A=
ENST00000685809.1:c.4505A= ENSP00000508863.1:p.Gln1502=
ENST00000686029.1:c.670A=
ENST00000686191.1:n.3792A=
ENST00000686222.1:c.*4014A= ENSP00000508737.1:n.*4014A=
ENST00000686321.1:c.688A=
ENST00000686427.1:c.*1527A= ENSP00000510379.1:n.*1527A=
ENST00000686758.1:n.2335A=
ENST00000686801.1:c.4580A= ENSP00000509915.1:p.Gln1527=
ENST00000686826.1:n.911A=
ENST00000687016.1:c.4493A= ENSP00000509074.1:p.Gln1498=
ENST00000687704.1:c.*2317A= ENSP00000510454.1:n.*2317A=
ENST00000688066.1:c.4592A= ENSP00000510782.1:p.Gln1531=
ENST00000688124.1:c.*3510A= ENSP00000510645.1:n.*3510A=
ENST00000688848.1:c.*3936A= ENSP00000509419.1:n.*3936A=
ENST00000688985.1:c.1593A= ENSP00000510477.1:n.1593A=
ENST00000689129.1:c.4517A= ENSP00000510414.1:p.Gln1506=
ENST00000689177.1:n.5864A=
ENST00000689849.1:c.688A=
ENST00000689981.1:c.4592A= ENSP00000509035.1:p.Gln1531=
ENST00000690369.1:n.4610A=
ENST00000690590.1:n.1639A=
ENST00000690990.1:c.4586A= ENSP00000510461.1:p.Gln1529=
ENST00000691233.1:c.4511A= ENSP00000509215.1:p.Gln1504=
ENST00000691306.1:c.690A=
ENST00000691345.1:n.2302+1111A=
ENST00000691792.1:c.4580A= ENSP00000509911.1:p.Gln1527=
ENST00000691959.1:n.5311A=
ENST00000692844.1:n.1676A=
ENST00000692946.1:c.688A=
ENST00000693052.1:c.4610A= ENSP00000509558.1:p.Gln1537=
ENST00000693289.1:n.1751A=
ENST00000693440.1:c.4589A= ENSP00000509462.1:p.Gln1530=
ENST00000693499.1:n.5517A=
ENST00000693591.1:n.3329A=
ENST00000380817.8:c.4592A= MANE Select ENSP00000370196.2:p.Gln1531=
ENST00000348911.10:c.4517A= ENSP00000252027.7:p.Gln1506=
ENST00000380817.7:c.4592A= ENSP00000370196.2:p.Gln1531=
ENST00000418590.3:c.192A=
ENST00000470434.1:n.733A=
NM_002972.3:c.4592A= NP_002963.2:p.Gln1531=
XM_005261931.1:c.4595A= XP_005261988.1:p.Gln1532=
XM_005261935.1:c.4514A= XP_005261992.1:p.Gln1505=
XM_011530707.1:c.4694A= XP_011529009.1:p.Gln1565=
XM_011530708.1:c.4646A= XP_011529010.1:p.Gln1549=
XM_011530709.1:c.4622A= XP_011529011.1:p.Gln1541=
XM_011530710.1:c.4619A= XP_011529012.1:p.Gln1540=
XM_011530711.1:c.4619A= XP_011529013.1:p.Gln1540=
XR_938344.1:n.4712A=
NM_001365819.1:c.4517A= NP_001352748.1:p.Gln1506=
XM_005261935.2:c.4514A= XP_005261992.1:p.Gln1505=
XM_011530709.2:c.4622A= XP_011529011.1:p.Gln1541=
XM_011530710.2:c.4619A= XP_011529012.1:p.Gln1540=
XM_017028905.2:c.4544A= XP_016884394.1:p.Gln1515=
NM_002972.4:c.4592A= MANE Select NP_002963.2:p.Gln1531=