Canonical Allele Identifier: CA2410864042
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455125G= , CM000684.2:g.50455125G= GRCh38
NC_000022.10:g.50893554G= , CM000684.1:g.50893554G= GRCh37
NC_000022.9:g.49240420G= NCBI36
NG_041810.1:g.24947C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4494C= ENSP00000252027.8:p.Pro1498=
ENST00000418590.4:c.204C= ENSP00000401538.2:p.Pro68=
ENST00000470434.2:n.975C=
ENST00000684986.1:c.4575C= ENSP00000509117.1:p.Pro1525=
ENST00000685180.1:n.2488+5409C=
ENST00000685390.1:n.2540C=
ENST00000685411.1:n.322C=
ENST00000685592.1:c.806C=
ENST00000685809.1:c.4485C= ENSP00000508863.1:p.Pro1495=
ENST00000686029.1:c.650C=
ENST00000686191.1:n.3772C=
ENST00000686222.1:c.*3994C= ENSP00000508737.1:n.*3994C=
ENST00000686321.1:c.668C=
ENST00000686427.1:c.*1507C= ENSP00000510379.1:n.*1507C=
ENST00000686758.1:n.2315C=
ENST00000686801.1:c.4560C= ENSP00000509915.1:p.Pro1520=
ENST00000686826.1:n.891C=
ENST00000687016.1:c.4473C= ENSP00000509074.1:p.Pro1491=
ENST00000687704.1:c.*2297C= ENSP00000510454.1:n.*2297C=
ENST00000688066.1:c.4572C= ENSP00000510782.1:p.Pro1524=
ENST00000688124.1:c.*3490C= ENSP00000510645.1:n.*3490C=
ENST00000688848.1:c.*3916C= ENSP00000509419.1:n.*3916C=
ENST00000688985.1:c.1573C= ENSP00000510477.1:n.1573C=
ENST00000689129.1:c.4497C= ENSP00000510414.1:p.Pro1499=
ENST00000689177.1:n.5844C=
ENST00000689849.1:c.668C=
ENST00000689981.1:c.4572C= ENSP00000509035.1:p.Pro1524=
ENST00000690369.1:n.4590C=
ENST00000690590.1:n.1619C=
ENST00000690990.1:c.4566C= ENSP00000510461.1:p.Pro1522=
ENST00000691233.1:c.4491C= ENSP00000509215.1:p.Pro1497=
ENST00000691306.1:c.670C=
ENST00000691345.1:n.2302+1091C=
ENST00000691792.1:c.4560C= ENSP00000509911.1:p.Pro1520=
ENST00000691959.1:n.5291C=
ENST00000692844.1:n.1656C=
ENST00000692946.1:c.668C=
ENST00000693052.1:c.4590C= ENSP00000509558.1:p.Pro1530=
ENST00000693289.1:n.1731C=
ENST00000693440.1:c.4569C= ENSP00000509462.1:p.Pro1523=
ENST00000693499.1:n.5497C=
ENST00000693591.1:n.3309C=
ENST00000380817.8:c.4572C= MANE Select ENSP00000370196.2:p.Pro1524=
ENST00000348911.10:c.4497C= ENSP00000252027.7:p.Pro1499=
ENST00000380817.7:c.4572C= ENSP00000370196.2:p.Pro1524=
ENST00000418590.3:c.172C=
ENST00000470434.1:n.713C=
NM_002972.3:c.4572C= NP_002963.2:p.Pro1524=
XM_005261931.1:c.4575C= XP_005261988.1:p.Pro1525=
XM_005261935.1:c.4494C= XP_005261992.1:p.Pro1498=
XM_011530707.1:c.4674C= XP_011529009.1:p.Pro1558=
XM_011530708.1:c.4626C= XP_011529010.1:p.Pro1542=
XM_011530709.1:c.4602C= XP_011529011.1:p.Pro1534=
XM_011530710.1:c.4599C= XP_011529012.1:p.Pro1533=
XM_011530711.1:c.4599C= XP_011529013.1:p.Pro1533=
XR_938344.1:n.4692C=
NM_001365819.1:c.4497C= NP_001352748.1:p.Pro1499=
XM_005261935.2:c.4494C= XP_005261992.1:p.Pro1498=
XM_011530709.2:c.4602C= XP_011529011.1:p.Pro1534=
XM_011530710.2:c.4599C= XP_011529012.1:p.Pro1533=
XM_017028905.2:c.4524C= XP_016884394.1:p.Pro1508=
NM_002972.4:c.4572C= MANE Select NP_002963.2:p.Pro1524=