Canonical Allele Identifier: CA10315870
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50447572T>C , CM000684.2:g.50447572T>C GRCh38
NC_000022.10:g.50886001T>C , CM000684.1:g.50886001T>C GRCh37
NC_000022.9:g.49232867T>C NCBI36
NG_041810.1:g.32500A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.5323A>G ENSP00000252027.8:p.Met1775Val
ENST00000418590.4:c.997A>G ENSP00000401538.2:p.Met333Val
ENST00000470434.2:n.1804A>G
ENST00000473724.2:n.540A>G
ENST00000684986.1:c.5404A>G ENSP00000509117.1:p.Met1802Val
ENST00000685180.1:n.2944A>G
ENST00000685390.1:n.3352A>G
ENST00000685411.1:n.1774A>G
ENST00000685459.1:c.553A>G ENSP00000509511.1:p.Met185Val
ENST00000685592.1:c.1651A>G
ENST00000685809.1:c.5314A>G ENSP00000508863.1:p.Met1772Val
ENST00000686191.1:n.4601A>G
ENST00000686222.1:c.*4823A>G ENSP00000508737.1:n.*4823A>G
ENST00000686321.1:c.1714A>G
ENST00000686427.1:c.*2333A>G ENSP00000510379.1:n.*2333A>G
ENST00000686758.1:n.3215A>G
ENST00000686801.1:c.*239A>G ENSP00000509915.1:n.*239A>G
ENST00000686826.1:n.1720A>G
ENST00000687016.1:c.5299A>G ENSP00000509074.1:p.Met1767Val
ENST00000687704.1:c.*3197A>G ENSP00000510454.1:n.*3197A>G
ENST00000688066.1:c.5401A>G ENSP00000510782.1:p.Met1801Val
ENST00000688124.1:c.*4302A>G ENSP00000510645.1:n.*4302A>G
ENST00000688381.1:c.553A>G ENSP00000508847.1:p.Met185Val
ENST00000688848.1:c.*4745A>G ENSP00000509419.1:n.*4745A>G
ENST00000688985.1:c.2402A>G ENSP00000510477.1:n.2402A>G
ENST00000689129.1:c.5326A>G ENSP00000510414.1:p.Met1776Val
ENST00000689177.1:n.6670A>G
ENST00000689849.1:c.1486A>G
ENST00000689981.1:c.5401A>G ENSP00000509035.1:p.Met1801Val
ENST00000690369.1:n.5419A>G
ENST00000690590.1:n.2448A>G
ENST00000690990.1:c.5395A>G ENSP00000510461.1:p.Met1799Val
ENST00000691233.1:c.5320A>G ENSP00000509215.1:p.Met1774Val
ENST00000691345.1:n.2660A>G
ENST00000691792.1:c.5386A>G ENSP00000509911.1:p.Met1796Val
ENST00000691959.1:n.6743A>G
ENST00000692844.1:n.2485A>G
ENST00000692946.1:c.1497A>G
ENST00000693052.1:c.5419A>G ENSP00000509558.1:p.Met1807Val
ENST00000693068.1:c.484A>G ENSP00000509997.1:p.Met162Val
ENST00000693440.1:c.5398A>G ENSP00000509462.1:p.Met1800Val
ENST00000693591.1:n.4209A>G
ENST00000380817.8:c.5401A>G MANE Select ENSP00000370196.2:p.Met1801Val
ENST00000348911.10:c.5326A>G ENSP00000252027.7:p.Met1776Val
ENST00000380817.7:c.5401A>G ENSP00000370196.2:p.Met1801Val
ENST00000418590.3:c.965A>G
ENST00000470434.1:n.1542A>G
ENST00000473724.1:n.38A>G
NM_002972.3:c.5401A>G NP_002963.2:p.Met1801Val
XM_005261931.1:c.5404A>G XP_005261988.1:p.Met1802Val
XM_005261935.1:c.5323A>G XP_005261992.1:p.Met1775Val
XM_011530707.1:c.5503A>G XP_011529009.1:p.Met1835Val
XM_011530708.1:c.5455A>G XP_011529010.1:p.Met1819Val
XM_011530709.1:c.5431A>G XP_011529011.1:p.Met1811Val
XM_011530710.1:c.5428A>G XP_011529012.1:p.Met1810Val
XM_011530711.1:c.5428A>G XP_011529013.1:p.Met1810Val
XR_938344.1:n.5521A>G
NM_001365819.1:c.5326A>G NP_001352748.1:p.Met1776Val
XM_005261935.2:c.5323A>G XP_005261992.1:p.Met1775Val
XM_011530709.2:c.5431A>G XP_011529011.1:p.Met1811Val
XM_011530710.2:c.5428A>G XP_011529012.1:p.Met1810Val
XM_017028905.2:c.5353A>G XP_016884394.1:p.Met1785Val
NM_002972.4:c.5401A>G MANE Select NP_002963.2:p.Met1801Val