Canonical Allele Identifier: CA2410863978
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455019G= , CM000684.2:g.50455019G= GRCh38
NC_000022.10:g.50893448G= , CM000684.1:g.50893448G= GRCh37
NC_000022.9:g.49240314G= NCBI36
NG_041810.1:g.25053C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4600C= ENSP00000252027.8:p.Leu1534=
ENST00000418590.4:c.310C= ENSP00000401538.2:p.Leu104=
ENST00000470434.2:n.1081C=
ENST00000684986.1:c.4681C= ENSP00000509117.1:p.Leu1561=
ENST00000685180.1:n.2488+5515C=
ENST00000685390.1:n.2646C=
ENST00000685411.1:n.428C=
ENST00000685592.1:c.912C=
ENST00000685809.1:c.4591C= ENSP00000508863.1:p.Leu1531=
ENST00000686029.1:c.756C=
ENST00000686191.1:n.3878C=
ENST00000686222.1:c.*4100C= ENSP00000508737.1:n.*4100C=
ENST00000686321.1:c.774C=
ENST00000686427.1:c.*1613C= ENSP00000510379.1:n.*1613C=
ENST00000686758.1:n.2421C=
ENST00000686801.1:c.4666C= ENSP00000509915.1:p.Leu1556=
ENST00000686826.1:n.997C=
ENST00000687016.1:c.4579C= ENSP00000509074.1:p.Leu1527=
ENST00000687704.1:c.*2403C= ENSP00000510454.1:n.*2403C=
ENST00000688066.1:c.4678C= ENSP00000510782.1:p.Leu1560=
ENST00000688124.1:c.*3596C= ENSP00000510645.1:n.*3596C=
ENST00000688848.1:c.*4022C= ENSP00000509419.1:n.*4022C=
ENST00000688985.1:c.1679C= ENSP00000510477.1:n.1679C=
ENST00000689129.1:c.4603C= ENSP00000510414.1:p.Leu1535=
ENST00000689177.1:n.5950C=
ENST00000689849.1:c.774C=
ENST00000689981.1:c.4678C= ENSP00000509035.1:p.Leu1560=
ENST00000690369.1:n.4696C=
ENST00000690590.1:n.1725C=
ENST00000690990.1:c.4672C= ENSP00000510461.1:p.Leu1558=
ENST00000691233.1:c.4597C= ENSP00000509215.1:p.Leu1533=
ENST00000691306.1:c.776C=
ENST00000691345.1:n.2302+1197C=
ENST00000691792.1:c.4666C= ENSP00000509911.1:p.Leu1556=
ENST00000691959.1:n.5397C=
ENST00000692844.1:n.1762C=
ENST00000692946.1:c.774C=
ENST00000693052.1:c.4696C= ENSP00000509558.1:p.Leu1566=
ENST00000693289.1:n.1837C=
ENST00000693440.1:c.4675C= ENSP00000509462.1:p.Leu1559=
ENST00000693499.1:n.5603C=
ENST00000693591.1:n.3415C=
ENST00000380817.8:c.4678C= MANE Select ENSP00000370196.2:p.Leu1560=
ENST00000348911.10:c.4603C= ENSP00000252027.7:p.Leu1535=
ENST00000380817.7:c.4678C= ENSP00000370196.2:p.Leu1560=
ENST00000418590.3:c.278C=
ENST00000470434.1:n.819C=
NM_002972.3:c.4678C= NP_002963.2:p.Leu1560=
XM_005261931.1:c.4681C= XP_005261988.1:p.Leu1561=
XM_005261935.1:c.4600C= XP_005261992.1:p.Leu1534=
XM_011530707.1:c.4780C= XP_011529009.1:p.Leu1594=
XM_011530708.1:c.4732C= XP_011529010.1:p.Leu1578=
XM_011530709.1:c.4708C= XP_011529011.1:p.Leu1570=
XM_011530710.1:c.4705C= XP_011529012.1:p.Leu1569=
XM_011530711.1:c.4705C= XP_011529013.1:p.Leu1569=
XR_938344.1:n.4798C=
NM_001365819.1:c.4603C= NP_001352748.1:p.Leu1535=
XM_005261935.2:c.4600C= XP_005261992.1:p.Leu1534=
XM_011530709.2:c.4708C= XP_011529011.1:p.Leu1570=
XM_011530710.2:c.4705C= XP_011529012.1:p.Leu1569=
XM_017028905.2:c.4630C= XP_016884394.1:p.Leu1544=
NM_002972.4:c.4678C= MANE Select NP_002963.2:p.Leu1560=