Canonical Allele Identifier: CA10316237

Gene: SBF1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455257G>A , CM000684.2:g.50455257G>A	GRCh38
NC_000022.10:g.50893686G>A , CM000684.1:g.50893686G>A	GRCh37
NC_000022.9:g.49240552G>A	NCBI36
NG_041810.1:g.24815C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4443C>T	ENSP00000252027.8:p.Pro1481=
ENST00000418590.4:c.153C>T	ENSP00000401538.2:p.Pro51=
ENST00000470434.2:n.843C>T
ENST00000684986.1:c.4524C>T	ENSP00000509117.1:p.Pro1508=
ENST00000685180.1:n.2488+5277C>T
ENST00000685390.1:n.2489C>T
ENST00000685411.1:n.190C>T
ENST00000685592.1:c.755C>T
ENST00000685809.1:c.4434C>T	ENSP00000508863.1:p.Pro1478=
ENST00000686029.1:c.599C>T
ENST00000686191.1:n.3721C>T
ENST00000686222.1:c.*3943C>T	ENSP00000508737.1:n.*3943C>T
ENST00000686321.1:c.617C>T
ENST00000686427.1:c.*1456C>T	ENSP00000510379.1:n.*1456C>T
ENST00000686758.1:n.2183C>T
ENST00000686801.1:c.4509C>T	ENSP00000509915.1:p.Pro1503=
ENST00000686826.1:n.840C>T
ENST00000687016.1:c.4422C>T	ENSP00000509074.1:p.Pro1474=
ENST00000687704.1:c.*2246C>T	ENSP00000510454.1:n.*2246C>T
ENST00000688066.1:c.4521C>T	ENSP00000510782.1:p.Pro1507=
ENST00000688124.1:c.*3439C>T	ENSP00000510645.1:n.*3439C>T
ENST00000688848.1:c.*3865C>T	ENSP00000509419.1:n.*3865C>T
ENST00000688985.1:c.1522C>T	ENSP00000510477.1:n.1522C>T
ENST00000689129.1:c.4446C>T	ENSP00000510414.1:p.Pro1482=
ENST00000689177.1:n.5793C>T
ENST00000689849.1:c.617C>T
ENST00000689981.1:c.4521C>T	ENSP00000509035.1:p.Pro1507=
ENST00000690369.1:n.4539C>T
ENST00000690590.1:n.1568C>T
ENST00000690990.1:c.4515C>T	ENSP00000510461.1:p.Pro1505=
ENST00000691233.1:c.4440C>T	ENSP00000509215.1:p.Pro1480=
ENST00000691306.1:c.619C>T
ENST00000691345.1:n.2302+959C>T
ENST00000691792.1:c.4521C>T	ENSP00000509911.1:p.Pro1507=
ENST00000691959.1:n.5240C>T
ENST00000692844.1:n.1605C>T
ENST00000692946.1:c.617C>T
ENST00000693052.1:c.4539C>T	ENSP00000509558.1:p.Pro1513=
ENST00000693289.1:n.1680C>T
ENST00000693440.1:c.4518C>T	ENSP00000509462.1:p.Pro1506=
ENST00000693499.1:n.5446C>T
ENST00000693591.1:n.3258C>T
ENST00000380817.8:c.4521C>T MANE Select	ENSP00000370196.2:p.Pro1507=
ENST00000348911.10:c.4446C>T	ENSP00000252027.7:p.Pro1482=
ENST00000380817.7:c.4521C>T	ENSP00000370196.2:p.Pro1507=
ENST00000418590.3:c.121C>T
ENST00000470434.1:n.662C>T
NM_002972.3:c.4521C>T	NP_002963.2:p.Pro1507=
XM_005261931.1:c.4524C>T	XP_005261988.1:p.Pro1508=
XM_005261935.1:c.4443C>T	XP_005261992.1:p.Pro1481=
XM_011530707.1:c.4623C>T	XP_011529009.1:p.Pro1541=
XM_011530708.1:c.4575C>T	XP_011529010.1:p.Pro1525=
XM_011530709.1:c.4551C>T	XP_011529011.1:p.Pro1517=
XM_011530710.1:c.4548C>T	XP_011529012.1:p.Pro1516=
XM_011530711.1:c.4548C>T	XP_011529013.1:p.Pro1516=
XR_938344.1:n.4641C>T
NM_001365819.1:c.4446C>T	NP_001352748.1:p.Pro1482=
XM_005261935.2:c.4443C>T	XP_005261992.1:p.Pro1481=
XM_011530709.2:c.4551C>T	XP_011529011.1:p.Pro1517=
XM_011530710.2:c.4548C>T	XP_011529012.1:p.Pro1516=
XM_017028905.2:c.4473C>T	XP_016884394.1:p.Pro1491=
NM_002972.4:c.4521C>T MANE Select	NP_002963.2:p.Pro1507=