Canonical Allele Identifier: CA2410864030
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455098G= , CM000684.2:g.50455098G= GRCh38
NC_000022.10:g.50893527G= , CM000684.1:g.50893527G= GRCh37
NC_000022.9:g.49240393G= NCBI36
NG_041810.1:g.24974C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4521C= ENSP00000252027.8:p.Tyr1507=
ENST00000418590.4:c.231C= ENSP00000401538.2:p.Tyr77=
ENST00000470434.2:n.1002C=
ENST00000684986.1:c.4602C= ENSP00000509117.1:p.Tyr1534=
ENST00000685180.1:n.2488+5436C=
ENST00000685390.1:n.2567C=
ENST00000685411.1:n.349C=
ENST00000685592.1:c.833C=
ENST00000685809.1:c.4512C= ENSP00000508863.1:p.Tyr1504=
ENST00000686029.1:c.677C=
ENST00000686191.1:n.3799C=
ENST00000686222.1:c.*4021C= ENSP00000508737.1:n.*4021C=
ENST00000686321.1:c.695C=
ENST00000686427.1:c.*1534C= ENSP00000510379.1:n.*1534C=
ENST00000686758.1:n.2342C=
ENST00000686801.1:c.4587C= ENSP00000509915.1:p.Tyr1529=
ENST00000686826.1:n.918C=
ENST00000687016.1:c.4500C= ENSP00000509074.1:p.Tyr1500=
ENST00000687704.1:c.*2324C= ENSP00000510454.1:n.*2324C=
ENST00000688066.1:c.4599C= ENSP00000510782.1:p.Tyr1533=
ENST00000688124.1:c.*3517C= ENSP00000510645.1:n.*3517C=
ENST00000688848.1:c.*3943C= ENSP00000509419.1:n.*3943C=
ENST00000688985.1:c.1600C= ENSP00000510477.1:n.1600C=
ENST00000689129.1:c.4524C= ENSP00000510414.1:p.Tyr1508=
ENST00000689177.1:n.5871C=
ENST00000689849.1:c.695C=
ENST00000689981.1:c.4599C= ENSP00000509035.1:p.Tyr1533=
ENST00000690369.1:n.4617C=
ENST00000690590.1:n.1646C=
ENST00000690990.1:c.4593C= ENSP00000510461.1:p.Tyr1531=
ENST00000691233.1:c.4518C= ENSP00000509215.1:p.Tyr1506=
ENST00000691306.1:c.697C=
ENST00000691345.1:n.2302+1118C=
ENST00000691792.1:c.4587C= ENSP00000509911.1:p.Tyr1529=
ENST00000691959.1:n.5318C=
ENST00000692844.1:n.1683C=
ENST00000692946.1:c.695C=
ENST00000693052.1:c.4617C= ENSP00000509558.1:p.Tyr1539=
ENST00000693289.1:n.1758C=
ENST00000693440.1:c.4596C= ENSP00000509462.1:p.Tyr1532=
ENST00000693499.1:n.5524C=
ENST00000693591.1:n.3336C=
ENST00000380817.8:c.4599C= MANE Select ENSP00000370196.2:p.Tyr1533=
ENST00000348911.10:c.4524C= ENSP00000252027.7:p.Tyr1508=
ENST00000380817.7:c.4599C= ENSP00000370196.2:p.Tyr1533=
ENST00000418590.3:c.199C=
ENST00000470434.1:n.740C=
NM_002972.3:c.4599C= NP_002963.2:p.Tyr1533=
XM_005261931.1:c.4602C= XP_005261988.1:p.Tyr1534=
XM_005261935.1:c.4521C= XP_005261992.1:p.Tyr1507=
XM_011530707.1:c.4701C= XP_011529009.1:p.Tyr1567=
XM_011530708.1:c.4653C= XP_011529010.1:p.Tyr1551=
XM_011530709.1:c.4629C= XP_011529011.1:p.Tyr1543=
XM_011530710.1:c.4626C= XP_011529012.1:p.Tyr1542=
XM_011530711.1:c.4626C= XP_011529013.1:p.Tyr1542=
XR_938344.1:n.4719C=
NM_001365819.1:c.4524C= NP_001352748.1:p.Tyr1508=
XM_005261935.2:c.4521C= XP_005261992.1:p.Tyr1507=
XM_011530709.2:c.4629C= XP_011529011.1:p.Tyr1543=
XM_011530710.2:c.4626C= XP_011529012.1:p.Tyr1542=
XM_017028905.2:c.4551C= XP_016884394.1:p.Tyr1517=
NM_002972.4:c.4599C= MANE Select NP_002963.2:p.Tyr1533=