Canonical Allele Identifier: CA412193629
Gene: SBF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50454926T>C , CM000684.2:g.50454926T>C GRCh38
NC_000022.10:g.50893355T>C , CM000684.1:g.50893355T>C GRCh37
NC_000022.9:g.49240221T>C NCBI36
NG_041810.1:g.25146A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4622A>G ENSP00000252027.8:p.Lys1541Arg
ENST00000418590.4:c.332A>G ENSP00000401538.2:p.Lys111Arg
ENST00000470434.2:n.1103A>G
ENST00000684986.1:c.4703A>G ENSP00000509117.1:p.Lys1568Arg
ENST00000685180.1:n.2488+5608A>G
ENST00000685390.1:n.2668A>G
ENST00000685411.1:n.450A>G
ENST00000685592.1:c.934A>G
ENST00000685809.1:c.4613A>G ENSP00000508863.1:p.Lys1538Arg
ENST00000686029.1:c.778A>G
ENST00000686191.1:n.3900A>G
ENST00000686222.1:c.*4122A>G ENSP00000508737.1:n.*4122A>G
ENST00000686321.1:c.796A>G
ENST00000686427.1:c.*1635A>G ENSP00000510379.1:n.*1635A>G
ENST00000686758.1:n.2514A>G
ENST00000686801.1:c.4688A>G ENSP00000509915.1:p.Lys1563Arg
ENST00000686826.1:n.1019A>G
ENST00000687016.1:c.4601A>G ENSP00000509074.1:p.Lys1534Arg
ENST00000687704.1:c.*2425A>G ENSP00000510454.1:n.*2425A>G
ENST00000688066.1:c.4700A>G ENSP00000510782.1:p.Lys1567Arg
ENST00000688124.1:c.*3618A>G ENSP00000510645.1:n.*3618A>G
ENST00000688848.1:c.*4044A>G ENSP00000509419.1:n.*4044A>G
ENST00000688985.1:c.1701A>G ENSP00000510477.1:n.1701A>G
ENST00000689129.1:c.4625A>G ENSP00000510414.1:p.Lys1542Arg
ENST00000689177.1:n.5972A>G
ENST00000689849.1:c.796A>G
ENST00000689981.1:c.4700A>G ENSP00000509035.1:p.Lys1567Arg
ENST00000690369.1:n.4718A>G
ENST00000690590.1:n.1747A>G
ENST00000690990.1:c.4694A>G ENSP00000510461.1:p.Lys1565Arg
ENST00000691233.1:c.4619A>G ENSP00000509215.1:p.Lys1540Arg
ENST00000691306.1:c.781A>G
ENST00000691345.1:n.2302+1290A>G
ENST00000691792.1:c.4688A>G ENSP00000509911.1:p.Lys1563Arg
ENST00000691959.1:n.5419A>G
ENST00000692844.1:n.1784A>G
ENST00000692946.1:c.796A>G
ENST00000693052.1:c.4718A>G ENSP00000509558.1:p.Lys1573Arg
ENST00000693289.1:n.1859A>G
ENST00000693440.1:c.4697A>G ENSP00000509462.1:p.Lys1566Arg
ENST00000693499.1:n.5696A>G
ENST00000693591.1:n.3508A>G
ENST00000380817.8:c.4700A>G MANE Select ENSP00000370196.2:p.Lys1567Arg
ENST00000348911.10:c.4625A>G ENSP00000252027.7:p.Lys1542Arg
ENST00000380817.7:c.4700A>G ENSP00000370196.2:p.Lys1567Arg
ENST00000418590.3:c.300A>G
ENST00000470434.1:n.841A>G
NM_002972.3:c.4700A>G NP_002963.2:p.Lys1567Arg
XM_005261931.1:c.4703A>G XP_005261988.1:p.Lys1568Arg
XM_005261935.1:c.4622A>G XP_005261992.1:p.Lys1541Arg
XM_011530707.1:c.4802A>G XP_011529009.1:p.Lys1601Arg
XM_011530708.1:c.4754A>G XP_011529010.1:p.Lys1585Arg
XM_011530709.1:c.4730A>G XP_011529011.1:p.Lys1577Arg
XM_011530710.1:c.4727A>G XP_011529012.1:p.Lys1576Arg
XM_011530711.1:c.4727A>G XP_011529013.1:p.Lys1576Arg
XR_938344.1:n.4820A>G
NM_001365819.1:c.4625A>G NP_001352748.1:p.Lys1542Arg
XM_005261935.2:c.4622A>G XP_005261992.1:p.Lys1541Arg
XM_011530709.2:c.4730A>G XP_011529011.1:p.Lys1577Arg
XM_011530710.2:c.4727A>G XP_011529012.1:p.Lys1576Arg
XM_017028905.2:c.4652A>G XP_016884394.1:p.Lys1551Arg
NM_002972.4:c.4700A>G MANE Select NP_002963.2:p.Lys1567Arg