Canonical Allele Identifier: CA10315930
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50448394C>A , CM000684.2:g.50448394C>A GRCh38
NC_000022.10:g.50886823C>A , CM000684.1:g.50886823C>A GRCh37
NC_000022.9:g.49233689C>A NCBI36
NG_041810.1:g.31678G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.5124G>T ENSP00000252027.8:p.Ser1708=
ENST00000418590.4:c.798G>T ENSP00000401538.2:p.Ser266=
ENST00000470434.2:n.1605G>T
ENST00000473724.2:n.341G>T
ENST00000684986.1:c.5205G>T ENSP00000509117.1:p.Ser1735=
ENST00000685180.1:n.2745G>T
ENST00000685390.1:n.3153G>T
ENST00000685411.1:n.952G>T
ENST00000685459.1:c.354G>T ENSP00000509511.1:p.Ser118=
ENST00000685592.1:c.1452G>T
ENST00000685809.1:c.5115G>T ENSP00000508863.1:p.Ser1705=
ENST00000686191.1:n.4402G>T
ENST00000686222.1:c.*4624G>T ENSP00000508737.1:n.*4624G>T
ENST00000686321.1:c.1298G>T
ENST00000686427.1:c.*2134G>T ENSP00000510379.1:n.*2134G>T
ENST00000686758.1:n.3016G>T
ENST00000686801.1:c.*40G>T ENSP00000509915.1:n.*40G>T
ENST00000686826.1:n.1521G>T
ENST00000687016.1:c.5100G>T ENSP00000509074.1:p.Ser1700=
ENST00000687704.1:c.*2998G>T ENSP00000510454.1:n.*2998G>T
ENST00000688066.1:c.5202G>T ENSP00000510782.1:p.Ser1734=
ENST00000688124.1:c.*4103G>T ENSP00000510645.1:n.*4103G>T
ENST00000688381.1:c.354G>T ENSP00000508847.1:p.Ser118=
ENST00000688848.1:c.*4546G>T ENSP00000509419.1:n.*4546G>T
ENST00000688985.1:c.2203G>T ENSP00000510477.1:n.2203G>T
ENST00000689129.1:c.5127G>T ENSP00000510414.1:p.Ser1709=
ENST00000689177.1:n.6471G>T
ENST00000689849.1:c.1287G>T
ENST00000689981.1:c.5202G>T ENSP00000509035.1:p.Ser1734=
ENST00000690369.1:n.5220G>T
ENST00000690590.1:n.2249G>T
ENST00000690990.1:c.5196G>T ENSP00000510461.1:p.Ser1732=
ENST00000691233.1:c.5121G>T ENSP00000509215.1:p.Ser1707=
ENST00000691345.1:n.2461G>T
ENST00000691792.1:c.5187G>T ENSP00000509911.1:p.Ser1729=
ENST00000691959.1:n.5921G>T
ENST00000692844.1:n.2286G>T
ENST00000692946.1:c.1298G>T
ENST00000693052.1:c.5220G>T ENSP00000509558.1:p.Ser1740=
ENST00000693068.1:c.304-19G>T ENSP00000509997.1:n.304-19G>T
ENST00000693440.1:c.5199G>T ENSP00000509462.1:p.Ser1733=
ENST00000693591.1:n.4010G>T
ENST00000380817.8:c.5202G>T MANE Select ENSP00000370196.2:p.Ser1734=
ENST00000348911.10:c.5127G>T ENSP00000252027.7:p.Ser1709=
ENST00000380817.7:c.5202G>T ENSP00000370196.2:p.Ser1734=
ENST00000418590.3:c.766G>T
ENST00000470434.1:n.1343G>T
NM_002972.3:c.5202G>T NP_002963.2:p.Ser1734=
XM_005261931.1:c.5205G>T XP_005261988.1:p.Ser1735=
XM_005261935.1:c.5124G>T XP_005261992.1:p.Ser1708=
XM_011530707.1:c.5304G>T XP_011529009.1:p.Ser1768=
XM_011530708.1:c.5256G>T XP_011529010.1:p.Ser1752=
XM_011530709.1:c.5232G>T XP_011529011.1:p.Ser1744=
XM_011530710.1:c.5229G>T XP_011529012.1:p.Ser1743=
XM_011530711.1:c.5229G>T XP_011529013.1:p.Ser1743=
XR_938344.1:n.5322G>T
NM_001365819.1:c.5127G>T NP_001352748.1:p.Ser1709=
XM_005261935.2:c.5124G>T XP_005261992.1:p.Ser1708=
XM_011530709.2:c.5232G>T XP_011529011.1:p.Ser1744=
XM_011530710.2:c.5229G>T XP_011529012.1:p.Ser1743=
XM_017028905.2:c.5154G>T XP_016884394.1:p.Ser1718=
NM_002972.4:c.5202G>T MANE Select NP_002963.2:p.Ser1734=