Canonical Allele Identifier: CA10316435
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50456564G>T , CM000684.2:g.50456564G>T GRCh38
NC_000022.10:g.50894993G>T , CM000684.1:g.50894993G>T GRCh37
NC_000022.9:g.49241859G>T NCBI36
NG_041810.1:g.23508C>A

Transcript Alleles

HGVS Amino-acid Change
NM_002972.4:c.4014C>A MANE Select NP_002963.2:p.Gly1338=
ENST00000380817.8:c.4014C>A MANE Select ENSP00000370196.2:p.Gly1338=
NM_001365819.1:c.3939C>A NP_001352748.1:p.Gly1313=
NM_002972.3:c.4014C>A NP_002963.2:p.Gly1338=
ENST00000348911.10:c.3939C>A ENSP00000252027.7:p.Gly1313=
ENST00000348911.11:c.3936C>A ENSP00000252027.8:p.Gly1312=
ENST00000380817.7:c.4014C>A ENSP00000370196.2:p.Gly1338=
ENST00000470434.2:n.336C>A
ENST00000684986.1:c.4017C>A ENSP00000509117.1:p.Gly1339=
ENST00000685180.1:n.2488+3970C>A
ENST00000685390.1:n.1982C>A
ENST00000685592.1:c.248C>A
ENST00000685809.1:c.3927C>A ENSP00000508863.1:p.Gly1309=
ENST00000686029.1:c.110C>A
ENST00000686191.1:n.3214C>A
ENST00000686222.1:c.*3436C>A ENSP00000508737.1:n.*3436C>A
ENST00000686321.1:c.110C>A
ENST00000686427.1:c.*949C>A ENSP00000510379.1:n.*949C>A
ENST00000686758.1:n.1676C>A
ENST00000686801.1:c.4002C>A ENSP00000509915.1:p.Gly1334=
ENST00000686826.1:n.331C>A
ENST00000687016.1:c.3915C>A ENSP00000509074.1:p.Gly1305=
ENST00000687704.1:c.*1739C>A ENSP00000510454.1:n.*1739C>A
ENST00000688066.1:c.4014C>A ENSP00000510782.1:p.Gly1338=
ENST00000688124.1:c.*2930C>A ENSP00000510645.1:n.*2930C>A
ENST00000688848.1:c.*3358C>A ENSP00000509419.1:n.*3358C>A
ENST00000688985.1:c.1015C>A ENSP00000510477.1:p.Pro339Thr
ENST00000689129.1:c.3939C>A ENSP00000510414.1:p.Gly1313=
ENST00000689177.1:n.4653C>A
ENST00000689849.1:c.110C>A
ENST00000689981.1:c.4014C>A ENSP00000509035.1:p.Gly1338=
ENST00000690369.1:n.4032C>A
ENST00000690590.1:n.1061C>A
ENST00000690990.1:c.4008C>A ENSP00000510461.1:p.Gly1336=
ENST00000691233.1:c.3933C>A ENSP00000509215.1:p.Gly1311=
ENST00000691306.1:c.110C>A
ENST00000691345.1:n.2050C>A
ENST00000691792.1:c.4014C>A ENSP00000509911.1:p.Gly1338=
ENST00000691959.1:n.4100C>A
ENST00000692844.1:n.1098C>A
ENST00000692946.1:c.110C>A
ENST00000693052.1:c.4032C>A ENSP00000509558.1:p.Gly1344=
ENST00000693289.1:n.1173C>A
ENST00000693440.1:c.4011C>A ENSP00000509462.1:p.Gly1337=
ENST00000693499.1:n.4939C>A
ENST00000693591.1:n.2118C>A
XM_005261931.1:c.4017C>A XP_005261988.1:p.Gly1339=
XM_005261935.1:c.3936C>A XP_005261992.1:p.Gly1312=
XM_005261935.2:c.3936C>A XP_005261992.1:p.Gly1312=
XM_011530707.1:c.4116C>A XP_011529009.1:p.Gly1372=
XM_011530708.1:c.4068C>A XP_011529010.1:p.Gly1356=
XM_011530709.1:c.4044C>A XP_011529011.1:p.Gly1348=
XM_011530709.2:c.4044C>A XP_011529011.1:p.Gly1348=
XM_011530710.1:c.4041C>A XP_011529012.1:p.Gly1347=
XM_011530710.2:c.4041C>A XP_011529012.1:p.Gly1347=
XM_011530711.1:c.4041C>A XP_011529013.1:p.Gly1347=
XM_017028905.2:c.3966C>A XP_016884394.1:p.Gly1322=
XR_938344.1:n.4134C>A