Canonical Allele Identifier: CA412195336

Gene: SBF1

Linked Data

• MyVariant Identifiers: chr22:g.50893541A>C (hg19) ; chr22:g.50455112A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455112A>C , CM000684.2:g.50455112A>C	GRCh38
NC_000022.10:g.50893541A>C , CM000684.1:g.50893541A>C	GRCh37
NC_000022.9:g.49240407A>C	NCBI36
NG_041810.1:g.24960T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4507T>G	ENSP00000252027.8:p.Phe1503Val
ENST00000418590.4:c.217T>G	ENSP00000401538.2:p.Phe73Val
ENST00000470434.2:n.988T>G
ENST00000684986.1:c.4588T>G	ENSP00000509117.1:p.Phe1530Val
ENST00000685180.1:n.2488+5422T>G
ENST00000685390.1:n.2553T>G
ENST00000685411.1:n.335T>G
ENST00000685592.1:c.819T>G
ENST00000685809.1:c.4498T>G	ENSP00000508863.1:p.Phe1500Val
ENST00000686029.1:c.663T>G
ENST00000686191.1:n.3785T>G
ENST00000686222.1:c.*4007T>G	ENSP00000508737.1:n.*4007T>G
ENST00000686321.1:c.681T>G
ENST00000686427.1:c.*1520T>G	ENSP00000510379.1:n.*1520T>G
ENST00000686758.1:n.2328T>G
ENST00000686801.1:c.4573T>G	ENSP00000509915.1:p.Phe1525Val
ENST00000686826.1:n.904T>G
ENST00000687016.1:c.4486T>G	ENSP00000509074.1:p.Phe1496Val
ENST00000687704.1:c.*2310T>G	ENSP00000510454.1:n.*2310T>G
ENST00000688066.1:c.4585T>G	ENSP00000510782.1:p.Phe1529Val
ENST00000688124.1:c.*3503T>G	ENSP00000510645.1:n.*3503T>G
ENST00000688848.1:c.*3929T>G	ENSP00000509419.1:n.*3929T>G
ENST00000688985.1:c.1586T>G	ENSP00000510477.1:n.1586T>G
ENST00000689129.1:c.4510T>G	ENSP00000510414.1:p.Phe1504Val
ENST00000689177.1:n.5857T>G
ENST00000689849.1:c.681T>G
ENST00000689981.1:c.4585T>G	ENSP00000509035.1:p.Phe1529Val
ENST00000690369.1:n.4603T>G
ENST00000690590.1:n.1632T>G
ENST00000690990.1:c.4579T>G	ENSP00000510461.1:p.Phe1527Val
ENST00000691233.1:c.4504T>G	ENSP00000509215.1:p.Phe1502Val
ENST00000691306.1:c.683T>G
ENST00000691345.1:n.2302+1104T>G
ENST00000691792.1:c.4573T>G	ENSP00000509911.1:p.Phe1525Val
ENST00000691959.1:n.5304T>G
ENST00000692844.1:n.1669T>G
ENST00000692946.1:c.681T>G
ENST00000693052.1:c.4603T>G	ENSP00000509558.1:p.Phe1535Val
ENST00000693289.1:n.1744T>G
ENST00000693440.1:c.4582T>G	ENSP00000509462.1:p.Phe1528Val
ENST00000693499.1:n.5510T>G
ENST00000693591.1:n.3322T>G
ENST00000380817.8:c.4585T>G MANE Select	ENSP00000370196.2:p.Phe1529Val
ENST00000348911.10:c.4510T>G	ENSP00000252027.7:p.Phe1504Val
ENST00000380817.7:c.4585T>G	ENSP00000370196.2:p.Phe1529Val
ENST00000418590.3:c.185T>G
ENST00000470434.1:n.726T>G
NM_002972.3:c.4585T>G	NP_002963.2:p.Phe1529Val
XM_005261931.1:c.4588T>G	XP_005261988.1:p.Phe1530Val
XM_005261935.1:c.4507T>G	XP_005261992.1:p.Phe1503Val
XM_011530707.1:c.4687T>G	XP_011529009.1:p.Phe1563Val
XM_011530708.1:c.4639T>G	XP_011529010.1:p.Phe1547Val
XM_011530709.1:c.4615T>G	XP_011529011.1:p.Phe1539Val
XM_011530710.1:c.4612T>G	XP_011529012.1:p.Phe1538Val
XM_011530711.1:c.4612T>G	XP_011529013.1:p.Phe1538Val
XR_938344.1:n.4705T>G
NM_001365819.1:c.4510T>G	NP_001352748.1:p.Phe1504Val
XM_005261935.2:c.4507T>G	XP_005261992.1:p.Phe1503Val
XM_011530709.2:c.4615T>G	XP_011529011.1:p.Phe1539Val
XM_011530710.2:c.4612T>G	XP_011529012.1:p.Phe1538Val
XM_017028905.2:c.4537T>G	XP_016884394.1:p.Phe1513Val
NM_002972.4:c.4585T>G MANE Select	NP_002963.2:p.Phe1529Val