Canonical Allele Identifier: CA2410864047
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455134C= , CM000684.2:g.50455134C= GRCh38
NC_000022.10:g.50893563C= , CM000684.1:g.50893563C= GRCh37
NC_000022.9:g.49240429C= NCBI36
NG_041810.1:g.24938G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4485G= ENSP00000252027.8:p.Leu1495=
ENST00000418590.4:c.195G= ENSP00000401538.2:p.Leu65=
ENST00000470434.2:n.966G=
ENST00000684986.1:c.4566G= ENSP00000509117.1:p.Leu1522=
ENST00000685180.1:n.2488+5400G=
ENST00000685390.1:n.2531G=
ENST00000685411.1:n.313G=
ENST00000685592.1:c.797G=
ENST00000685809.1:c.4476G= ENSP00000508863.1:p.Leu1492=
ENST00000686029.1:c.641G=
ENST00000686191.1:n.3763G=
ENST00000686222.1:c.*3985G= ENSP00000508737.1:n.*3985G=
ENST00000686321.1:c.659G=
ENST00000686427.1:c.*1498G= ENSP00000510379.1:n.*1498G=
ENST00000686758.1:n.2306G=
ENST00000686801.1:c.4551G= ENSP00000509915.1:p.Leu1517=
ENST00000686826.1:n.882G=
ENST00000687016.1:c.4464G= ENSP00000509074.1:p.Leu1488=
ENST00000687704.1:c.*2288G= ENSP00000510454.1:n.*2288G=
ENST00000688066.1:c.4563G= ENSP00000510782.1:p.Leu1521=
ENST00000688124.1:c.*3481G= ENSP00000510645.1:n.*3481G=
ENST00000688848.1:c.*3907G= ENSP00000509419.1:n.*3907G=
ENST00000688985.1:c.1564G= ENSP00000510477.1:n.1564G=
ENST00000689129.1:c.4488G= ENSP00000510414.1:p.Leu1496=
ENST00000689177.1:n.5835G=
ENST00000689849.1:c.659G=
ENST00000689981.1:c.4563G= ENSP00000509035.1:p.Leu1521=
ENST00000690369.1:n.4581G=
ENST00000690590.1:n.1610G=
ENST00000690990.1:c.4557G= ENSP00000510461.1:p.Leu1519=
ENST00000691233.1:c.4482G= ENSP00000509215.1:p.Leu1494=
ENST00000691306.1:c.661G=
ENST00000691345.1:n.2302+1082G=
ENST00000691792.1:c.4555-4G= ENSP00000509911.1:n.4555-4G=
ENST00000691959.1:n.5282G=
ENST00000692844.1:n.1647G=
ENST00000692946.1:c.659G=
ENST00000693052.1:c.4581G= ENSP00000509558.1:p.Leu1527=
ENST00000693289.1:n.1722G=
ENST00000693440.1:c.4560G= ENSP00000509462.1:p.Leu1520=
ENST00000693499.1:n.5488G=
ENST00000693591.1:n.3300G=
ENST00000380817.8:c.4563G= MANE Select ENSP00000370196.2:p.Leu1521=
ENST00000348911.10:c.4488G= ENSP00000252027.7:p.Leu1496=
ENST00000380817.7:c.4563G= ENSP00000370196.2:p.Leu1521=
ENST00000418590.3:c.163G=
ENST00000470434.1:n.704G=
NM_002972.3:c.4563G= NP_002963.2:p.Leu1521=
XM_005261931.1:c.4566G= XP_005261988.1:p.Leu1522=
XM_005261935.1:c.4485G= XP_005261992.1:p.Leu1495=
XM_011530707.1:c.4665G= XP_011529009.1:p.Leu1555=
XM_011530708.1:c.4617G= XP_011529010.1:p.Leu1539=
XM_011530709.1:c.4593G= XP_011529011.1:p.Leu1531=
XM_011530710.1:c.4590G= XP_011529012.1:p.Leu1530=
XM_011530711.1:c.4590G= XP_011529013.1:p.Leu1530=
XR_938344.1:n.4683G=
NM_001365819.1:c.4488G= NP_001352748.1:p.Leu1496=
XM_005261935.2:c.4485G= XP_005261992.1:p.Leu1495=
XM_011530709.2:c.4593G= XP_011529011.1:p.Leu1531=
XM_011530710.2:c.4590G= XP_011529012.1:p.Leu1530=
XM_017028905.2:c.4515G= XP_016884394.1:p.Leu1505=
NM_002972.4:c.4563G= MANE Select NP_002963.2:p.Leu1521=