Canonical Allele Identifier: CA412195333

Gene: SBF1

Linked Data

• MyVariant Identifiers: chr22:g.50893540A>G (hg19) ; chr22:g.50455111A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455111A>G , CM000684.2:g.50455111A>G	GRCh38
NC_000022.10:g.50893540A>G , CM000684.1:g.50893540A>G	GRCh37
NC_000022.9:g.49240406A>G	NCBI36
NG_041810.1:g.24961T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4508T>C	ENSP00000252027.8:p.Phe1503Ser
ENST00000418590.4:c.218T>C	ENSP00000401538.2:p.Phe73Ser
ENST00000470434.2:n.989T>C
ENST00000684986.1:c.4589T>C	ENSP00000509117.1:p.Phe1530Ser
ENST00000685180.1:n.2488+5423T>C
ENST00000685390.1:n.2554T>C
ENST00000685411.1:n.336T>C
ENST00000685592.1:c.820T>C
ENST00000685809.1:c.4499T>C	ENSP00000508863.1:p.Phe1500Ser
ENST00000686029.1:c.664T>C
ENST00000686191.1:n.3786T>C
ENST00000686222.1:c.*4008T>C	ENSP00000508737.1:n.*4008T>C
ENST00000686321.1:c.682T>C
ENST00000686427.1:c.*1521T>C	ENSP00000510379.1:n.*1521T>C
ENST00000686758.1:n.2329T>C
ENST00000686801.1:c.4574T>C	ENSP00000509915.1:p.Phe1525Ser
ENST00000686826.1:n.905T>C
ENST00000687016.1:c.4487T>C	ENSP00000509074.1:p.Phe1496Ser
ENST00000687704.1:c.*2311T>C	ENSP00000510454.1:n.*2311T>C
ENST00000688066.1:c.4586T>C	ENSP00000510782.1:p.Phe1529Ser
ENST00000688124.1:c.*3504T>C	ENSP00000510645.1:n.*3504T>C
ENST00000688848.1:c.*3930T>C	ENSP00000509419.1:n.*3930T>C
ENST00000688985.1:c.1587T>C	ENSP00000510477.1:n.1587T>C
ENST00000689129.1:c.4511T>C	ENSP00000510414.1:p.Phe1504Ser
ENST00000689177.1:n.5858T>C
ENST00000689849.1:c.682T>C
ENST00000689981.1:c.4586T>C	ENSP00000509035.1:p.Phe1529Ser
ENST00000690369.1:n.4604T>C
ENST00000690590.1:n.1633T>C
ENST00000690990.1:c.4580T>C	ENSP00000510461.1:p.Phe1527Ser
ENST00000691233.1:c.4505T>C	ENSP00000509215.1:p.Phe1502Ser
ENST00000691306.1:c.684T>C
ENST00000691345.1:n.2302+1105T>C
ENST00000691792.1:c.4574T>C	ENSP00000509911.1:p.Phe1525Ser
ENST00000691959.1:n.5305T>C
ENST00000692844.1:n.1670T>C
ENST00000692946.1:c.682T>C
ENST00000693052.1:c.4604T>C	ENSP00000509558.1:p.Phe1535Ser
ENST00000693289.1:n.1745T>C
ENST00000693440.1:c.4583T>C	ENSP00000509462.1:p.Phe1528Ser
ENST00000693499.1:n.5511T>C
ENST00000693591.1:n.3323T>C
ENST00000380817.8:c.4586T>C MANE Select	ENSP00000370196.2:p.Phe1529Ser
ENST00000348911.10:c.4511T>C	ENSP00000252027.7:p.Phe1504Ser
ENST00000380817.7:c.4586T>C	ENSP00000370196.2:p.Phe1529Ser
ENST00000418590.3:c.186T>C
ENST00000470434.1:n.727T>C
NM_002972.3:c.4586T>C	NP_002963.2:p.Phe1529Ser
XM_005261931.1:c.4589T>C	XP_005261988.1:p.Phe1530Ser
XM_005261935.1:c.4508T>C	XP_005261992.1:p.Phe1503Ser
XM_011530707.1:c.4688T>C	XP_011529009.1:p.Phe1563Ser
XM_011530708.1:c.4640T>C	XP_011529010.1:p.Phe1547Ser
XM_011530709.1:c.4616T>C	XP_011529011.1:p.Phe1539Ser
XM_011530710.1:c.4613T>C	XP_011529012.1:p.Phe1538Ser
XM_011530711.1:c.4613T>C	XP_011529013.1:p.Phe1538Ser
XR_938344.1:n.4706T>C
NM_001365819.1:c.4511T>C	NP_001352748.1:p.Phe1504Ser
XM_005261935.2:c.4508T>C	XP_005261992.1:p.Phe1503Ser
XM_011530709.2:c.4616T>C	XP_011529011.1:p.Phe1539Ser
XM_011530710.2:c.4613T>C	XP_011529012.1:p.Phe1538Ser
XM_017028905.2:c.4538T>C	XP_016884394.1:p.Phe1513Ser
NM_002972.4:c.4586T>C MANE Select	NP_002963.2:p.Phe1529Ser