Canonical Allele Identifier: CA2410864045
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455128G= , CM000684.2:g.50455128G= GRCh38
NC_000022.10:g.50893557G= , CM000684.1:g.50893557G= GRCh37
NC_000022.9:g.49240423G= NCBI36
NG_041810.1:g.24944C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4491C= ENSP00000252027.8:p.Phe1497=
ENST00000418590.4:c.201C= ENSP00000401538.2:p.Phe67=
ENST00000470434.2:n.972C=
ENST00000684986.1:c.4572C= ENSP00000509117.1:p.Phe1524=
ENST00000685180.1:n.2488+5406C=
ENST00000685390.1:n.2537C=
ENST00000685411.1:n.319C=
ENST00000685592.1:c.803C=
ENST00000685809.1:c.4482C= ENSP00000508863.1:p.Phe1494=
ENST00000686029.1:c.647C=
ENST00000686191.1:n.3769C=
ENST00000686222.1:c.*3991C= ENSP00000508737.1:n.*3991C=
ENST00000686321.1:c.665C=
ENST00000686427.1:c.*1504C= ENSP00000510379.1:n.*1504C=
ENST00000686758.1:n.2312C=
ENST00000686801.1:c.4557C= ENSP00000509915.1:p.Phe1519=
ENST00000686826.1:n.888C=
ENST00000687016.1:c.4470C= ENSP00000509074.1:p.Phe1490=
ENST00000687704.1:c.*2294C= ENSP00000510454.1:n.*2294C=
ENST00000688066.1:c.4569C= ENSP00000510782.1:p.Phe1523=
ENST00000688124.1:c.*3487C= ENSP00000510645.1:n.*3487C=
ENST00000688848.1:c.*3913C= ENSP00000509419.1:n.*3913C=
ENST00000688985.1:c.1570C= ENSP00000510477.1:n.1570C=
ENST00000689129.1:c.4494C= ENSP00000510414.1:p.Phe1498=
ENST00000689177.1:n.5841C=
ENST00000689849.1:c.665C=
ENST00000689981.1:c.4569C= ENSP00000509035.1:p.Phe1523=
ENST00000690369.1:n.4587C=
ENST00000690590.1:n.1616C=
ENST00000690990.1:c.4563C= ENSP00000510461.1:p.Phe1521=
ENST00000691233.1:c.4488C= ENSP00000509215.1:p.Phe1496=
ENST00000691306.1:c.667C=
ENST00000691345.1:n.2302+1088C=
ENST00000691792.1:c.4557C= ENSP00000509911.1:p.Phe1519=
ENST00000691959.1:n.5288C=
ENST00000692844.1:n.1653C=
ENST00000692946.1:c.665C=
ENST00000693052.1:c.4587C= ENSP00000509558.1:p.Phe1529=
ENST00000693289.1:n.1728C=
ENST00000693440.1:c.4566C= ENSP00000509462.1:p.Phe1522=
ENST00000693499.1:n.5494C=
ENST00000693591.1:n.3306C=
ENST00000380817.8:c.4569C= MANE Select ENSP00000370196.2:p.Phe1523=
ENST00000348911.10:c.4494C= ENSP00000252027.7:p.Phe1498=
ENST00000380817.7:c.4569C= ENSP00000370196.2:p.Phe1523=
ENST00000418590.3:c.169C=
ENST00000470434.1:n.710C=
NM_002972.3:c.4569C= NP_002963.2:p.Phe1523=
XM_005261931.1:c.4572C= XP_005261988.1:p.Phe1524=
XM_005261935.1:c.4491C= XP_005261992.1:p.Phe1497=
XM_011530707.1:c.4671C= XP_011529009.1:p.Phe1557=
XM_011530708.1:c.4623C= XP_011529010.1:p.Phe1541=
XM_011530709.1:c.4599C= XP_011529011.1:p.Phe1533=
XM_011530710.1:c.4596C= XP_011529012.1:p.Phe1532=
XM_011530711.1:c.4596C= XP_011529013.1:p.Phe1532=
XR_938344.1:n.4689C=
NM_001365819.1:c.4494C= NP_001352748.1:p.Phe1498=
XM_005261935.2:c.4491C= XP_005261992.1:p.Phe1497=
XM_011530709.2:c.4599C= XP_011529011.1:p.Phe1533=
XM_011530710.2:c.4596C= XP_011529012.1:p.Phe1532=
XM_017028905.2:c.4521C= XP_016884394.1:p.Phe1507=
NM_002972.4:c.4569C= MANE Select NP_002963.2:p.Phe1523=