Canonical Allele Identifier: CA2410864044
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455127G= , CM000684.2:g.50455127G= GRCh38
NC_000022.10:g.50893556G= , CM000684.1:g.50893556G= GRCh37
NC_000022.9:g.49240422G= NCBI36
NG_041810.1:g.24945C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4492C= ENSP00000252027.8:p.Pro1498=
ENST00000418590.4:c.202C= ENSP00000401538.2:p.Pro68=
ENST00000470434.2:n.973C=
ENST00000684986.1:c.4573C= ENSP00000509117.1:p.Pro1525=
ENST00000685180.1:n.2488+5407C=
ENST00000685390.1:n.2538C=
ENST00000685411.1:n.320C=
ENST00000685592.1:c.804C=
ENST00000685809.1:c.4483C= ENSP00000508863.1:p.Pro1495=
ENST00000686029.1:c.648C=
ENST00000686191.1:n.3770C=
ENST00000686222.1:c.*3992C= ENSP00000508737.1:n.*3992C=
ENST00000686321.1:c.666C=
ENST00000686427.1:c.*1505C= ENSP00000510379.1:n.*1505C=
ENST00000686758.1:n.2313C=
ENST00000686801.1:c.4558C= ENSP00000509915.1:p.Pro1520=
ENST00000686826.1:n.889C=
ENST00000687016.1:c.4471C= ENSP00000509074.1:p.Pro1491=
ENST00000687704.1:c.*2295C= ENSP00000510454.1:n.*2295C=
ENST00000688066.1:c.4570C= ENSP00000510782.1:p.Pro1524=
ENST00000688124.1:c.*3488C= ENSP00000510645.1:n.*3488C=
ENST00000688848.1:c.*3914C= ENSP00000509419.1:n.*3914C=
ENST00000688985.1:c.1571C= ENSP00000510477.1:n.1571C=
ENST00000689129.1:c.4495C= ENSP00000510414.1:p.Pro1499=
ENST00000689177.1:n.5842C=
ENST00000689849.1:c.666C=
ENST00000689981.1:c.4570C= ENSP00000509035.1:p.Pro1524=
ENST00000690369.1:n.4588C=
ENST00000690590.1:n.1617C=
ENST00000690990.1:c.4564C= ENSP00000510461.1:p.Pro1522=
ENST00000691233.1:c.4489C= ENSP00000509215.1:p.Pro1497=
ENST00000691306.1:c.668C=
ENST00000691345.1:n.2302+1089C=
ENST00000691792.1:c.4558C= ENSP00000509911.1:p.Pro1520=
ENST00000691959.1:n.5289C=
ENST00000692844.1:n.1654C=
ENST00000692946.1:c.666C=
ENST00000693052.1:c.4588C= ENSP00000509558.1:p.Pro1530=
ENST00000693289.1:n.1729C=
ENST00000693440.1:c.4567C= ENSP00000509462.1:p.Pro1523=
ENST00000693499.1:n.5495C=
ENST00000693591.1:n.3307C=
ENST00000380817.8:c.4570C= MANE Select ENSP00000370196.2:p.Pro1524=
ENST00000348911.10:c.4495C= ENSP00000252027.7:p.Pro1499=
ENST00000380817.7:c.4570C= ENSP00000370196.2:p.Pro1524=
ENST00000418590.3:c.170C=
ENST00000470434.1:n.711C=
NM_002972.3:c.4570C= NP_002963.2:p.Pro1524=
XM_005261931.1:c.4573C= XP_005261988.1:p.Pro1525=
XM_005261935.1:c.4492C= XP_005261992.1:p.Pro1498=
XM_011530707.1:c.4672C= XP_011529009.1:p.Pro1558=
XM_011530708.1:c.4624C= XP_011529010.1:p.Pro1542=
XM_011530709.1:c.4600C= XP_011529011.1:p.Pro1534=
XM_011530710.1:c.4597C= XP_011529012.1:p.Pro1533=
XM_011530711.1:c.4597C= XP_011529013.1:p.Pro1533=
XR_938344.1:n.4690C=
NM_001365819.1:c.4495C= NP_001352748.1:p.Pro1499=
XM_005261935.2:c.4492C= XP_005261992.1:p.Pro1498=
XM_011530709.2:c.4600C= XP_011529011.1:p.Pro1534=
XM_011530710.2:c.4597C= XP_011529012.1:p.Pro1533=
XM_017028905.2:c.4522C= XP_016884394.1:p.Pro1508=
NM_002972.4:c.4570C= MANE Select NP_002963.2:p.Pro1524=