Canonical Allele Identifier: CA2410864048
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455135A= , CM000684.2:g.50455135A= GRCh38
NC_000022.10:g.50893564A= , CM000684.1:g.50893564A= GRCh37
NC_000022.9:g.49240430A= NCBI36
NG_041810.1:g.24937T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4484T= ENSP00000252027.8:p.Leu1495=
ENST00000418590.4:c.194T= ENSP00000401538.2:p.Leu65=
ENST00000470434.2:n.965T=
ENST00000684986.1:c.4565T= ENSP00000509117.1:p.Leu1522=
ENST00000685180.1:n.2488+5399T=
ENST00000685390.1:n.2530T=
ENST00000685411.1:n.312T=
ENST00000685592.1:c.796T=
ENST00000685809.1:c.4475T= ENSP00000508863.1:p.Leu1492=
ENST00000686029.1:c.640T=
ENST00000686191.1:n.3762T=
ENST00000686222.1:c.*3984T= ENSP00000508737.1:n.*3984T=
ENST00000686321.1:c.658T=
ENST00000686427.1:c.*1497T= ENSP00000510379.1:n.*1497T=
ENST00000686758.1:n.2305T=
ENST00000686801.1:c.4550T= ENSP00000509915.1:p.Leu1517=
ENST00000686826.1:n.881T=
ENST00000687016.1:c.4463T= ENSP00000509074.1:p.Leu1488=
ENST00000687704.1:c.*2287T= ENSP00000510454.1:n.*2287T=
ENST00000688066.1:c.4562T= ENSP00000510782.1:p.Leu1521=
ENST00000688124.1:c.*3480T= ENSP00000510645.1:n.*3480T=
ENST00000688848.1:c.*3906T= ENSP00000509419.1:n.*3906T=
ENST00000688985.1:c.1563T= ENSP00000510477.1:n.1563T=
ENST00000689129.1:c.4487T= ENSP00000510414.1:p.Leu1496=
ENST00000689177.1:n.5834T=
ENST00000689849.1:c.658T=
ENST00000689981.1:c.4562T= ENSP00000509035.1:p.Leu1521=
ENST00000690369.1:n.4580T=
ENST00000690590.1:n.1609T=
ENST00000690990.1:c.4556T= ENSP00000510461.1:p.Leu1519=
ENST00000691233.1:c.4481T= ENSP00000509215.1:p.Leu1494=
ENST00000691306.1:c.660T=
ENST00000691345.1:n.2302+1081T=
ENST00000691792.1:c.4555-5T= ENSP00000509911.1:n.4555-5T=
ENST00000691959.1:n.5281T=
ENST00000692844.1:n.1646T=
ENST00000692946.1:c.658T=
ENST00000693052.1:c.4580T= ENSP00000509558.1:p.Leu1527=
ENST00000693289.1:n.1721T=
ENST00000693440.1:c.4559T= ENSP00000509462.1:p.Leu1520=
ENST00000693499.1:n.5487T=
ENST00000693591.1:n.3299T=
ENST00000380817.8:c.4562T= MANE Select ENSP00000370196.2:p.Leu1521=
ENST00000348911.10:c.4487T= ENSP00000252027.7:p.Leu1496=
ENST00000380817.7:c.4562T= ENSP00000370196.2:p.Leu1521=
ENST00000418590.3:c.162T=
ENST00000470434.1:n.703T=
NM_002972.3:c.4562T= NP_002963.2:p.Leu1521=
XM_005261931.1:c.4565T= XP_005261988.1:p.Leu1522=
XM_005261935.1:c.4484T= XP_005261992.1:p.Leu1495=
XM_011530707.1:c.4664T= XP_011529009.1:p.Leu1555=
XM_011530708.1:c.4616T= XP_011529010.1:p.Leu1539=
XM_011530709.1:c.4592T= XP_011529011.1:p.Leu1531=
XM_011530710.1:c.4589T= XP_011529012.1:p.Leu1530=
XM_011530711.1:c.4589T= XP_011529013.1:p.Leu1530=
XR_938344.1:n.4682T=
NM_001365819.1:c.4487T= NP_001352748.1:p.Leu1496=
XM_005261935.2:c.4484T= XP_005261992.1:p.Leu1495=
XM_011530709.2:c.4592T= XP_011529011.1:p.Leu1531=
XM_011530710.2:c.4589T= XP_011529012.1:p.Leu1530=
XM_017028905.2:c.4514T= XP_016884394.1:p.Leu1505=
NM_002972.4:c.4562T= MANE Select NP_002963.2:p.Leu1521=