Canonical Allele Identifier: CA2410864017
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455082A= , CM000684.2:g.50455082A= GRCh38
NC_000022.10:g.50893511A= , CM000684.1:g.50893511A= GRCh37
NC_000022.9:g.49240377A= NCBI36
NG_041810.1:g.24990T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4537T= ENSP00000252027.8:p.Tyr1513=
ENST00000418590.4:c.247T= ENSP00000401538.2:p.Tyr83=
ENST00000470434.2:n.1018T=
ENST00000684986.1:c.4618T= ENSP00000509117.1:p.Tyr1540=
ENST00000685180.1:n.2488+5452T=
ENST00000685390.1:n.2583T=
ENST00000685411.1:n.365T=
ENST00000685592.1:c.849T=
ENST00000685809.1:c.4528T= ENSP00000508863.1:p.Tyr1510=
ENST00000686029.1:c.693T=
ENST00000686191.1:n.3815T=
ENST00000686222.1:c.*4037T= ENSP00000508737.1:n.*4037T=
ENST00000686321.1:c.711T=
ENST00000686427.1:c.*1550T= ENSP00000510379.1:n.*1550T=
ENST00000686758.1:n.2358T=
ENST00000686801.1:c.4603T= ENSP00000509915.1:p.Tyr1535=
ENST00000686826.1:n.934T=
ENST00000687016.1:c.4516T= ENSP00000509074.1:p.Tyr1506=
ENST00000687704.1:c.*2340T= ENSP00000510454.1:n.*2340T=
ENST00000688066.1:c.4615T= ENSP00000510782.1:p.Tyr1539=
ENST00000688124.1:c.*3533T= ENSP00000510645.1:n.*3533T=
ENST00000688848.1:c.*3959T= ENSP00000509419.1:n.*3959T=
ENST00000688985.1:c.1616T= ENSP00000510477.1:n.1616T=
ENST00000689129.1:c.4540T= ENSP00000510414.1:p.Tyr1514=
ENST00000689177.1:n.5887T=
ENST00000689849.1:c.711T=
ENST00000689981.1:c.4615T= ENSP00000509035.1:p.Tyr1539=
ENST00000690369.1:n.4633T=
ENST00000690590.1:n.1662T=
ENST00000690990.1:c.4609T= ENSP00000510461.1:p.Tyr1537=
ENST00000691233.1:c.4534T= ENSP00000509215.1:p.Tyr1512=
ENST00000691306.1:c.713T=
ENST00000691345.1:n.2302+1134T=
ENST00000691792.1:c.4603T= ENSP00000509911.1:p.Tyr1535=
ENST00000691959.1:n.5334T=
ENST00000692844.1:n.1699T=
ENST00000692946.1:c.711T=
ENST00000693052.1:c.4633T= ENSP00000509558.1:p.Tyr1545=
ENST00000693289.1:n.1774T=
ENST00000693440.1:c.4612T= ENSP00000509462.1:p.Tyr1538=
ENST00000693499.1:n.5540T=
ENST00000693591.1:n.3352T=
ENST00000380817.8:c.4615T= MANE Select ENSP00000370196.2:p.Tyr1539=
ENST00000348911.10:c.4540T= ENSP00000252027.7:p.Tyr1514=
ENST00000380817.7:c.4615T= ENSP00000370196.2:p.Tyr1539=
ENST00000418590.3:c.215T=
ENST00000470434.1:n.756T=
NM_002972.3:c.4615T= NP_002963.2:p.Tyr1539=
XM_005261931.1:c.4618T= XP_005261988.1:p.Tyr1540=
XM_005261935.1:c.4537T= XP_005261992.1:p.Tyr1513=
XM_011530707.1:c.4717T= XP_011529009.1:p.Tyr1573=
XM_011530708.1:c.4669T= XP_011529010.1:p.Tyr1557=
XM_011530709.1:c.4645T= XP_011529011.1:p.Tyr1549=
XM_011530710.1:c.4642T= XP_011529012.1:p.Tyr1548=
XM_011530711.1:c.4642T= XP_011529013.1:p.Tyr1548=
XR_938344.1:n.4735T=
NM_001365819.1:c.4540T= NP_001352748.1:p.Tyr1514=
XM_005261935.2:c.4537T= XP_005261992.1:p.Tyr1513=
XM_011530709.2:c.4645T= XP_011529011.1:p.Tyr1549=
XM_011530710.2:c.4642T= XP_011529012.1:p.Tyr1548=
XM_017028905.2:c.4567T= XP_016884394.1:p.Tyr1523=
NM_002972.4:c.4615T= MANE Select NP_002963.2:p.Tyr1539=