Canonical Allele Identifier: CA412195403

Gene: SBF1

Linked Data

• MyVariant Identifiers: chr22:g.50893559A>C (hg19) ; chr22:g.50455130A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455130A>C , CM000684.2:g.50455130A>C	GRCh38
NC_000022.10:g.50893559A>C , CM000684.1:g.50893559A>C	GRCh37
NC_000022.9:g.49240425A>C	NCBI36
NG_041810.1:g.24942T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4489T>G	ENSP00000252027.8:p.Phe1497Val
ENST00000418590.4:c.199T>G	ENSP00000401538.2:p.Phe67Val
ENST00000470434.2:n.970T>G
ENST00000684986.1:c.4570T>G	ENSP00000509117.1:p.Phe1524Val
ENST00000685180.1:n.2488+5404T>G
ENST00000685390.1:n.2535T>G
ENST00000685411.1:n.317T>G
ENST00000685592.1:c.801T>G
ENST00000685809.1:c.4480T>G	ENSP00000508863.1:p.Phe1494Val
ENST00000686029.1:c.645T>G
ENST00000686191.1:n.3767T>G
ENST00000686222.1:c.*3989T>G	ENSP00000508737.1:n.*3989T>G
ENST00000686321.1:c.663T>G
ENST00000686427.1:c.*1502T>G	ENSP00000510379.1:n.*1502T>G
ENST00000686758.1:n.2310T>G
ENST00000686801.1:c.4555T>G	ENSP00000509915.1:p.Phe1519Val
ENST00000686826.1:n.886T>G
ENST00000687016.1:c.4468T>G	ENSP00000509074.1:p.Phe1490Val
ENST00000687704.1:c.*2292T>G	ENSP00000510454.1:n.*2292T>G
ENST00000688066.1:c.4567T>G	ENSP00000510782.1:p.Phe1523Val
ENST00000688124.1:c.*3485T>G	ENSP00000510645.1:n.*3485T>G
ENST00000688848.1:c.*3911T>G	ENSP00000509419.1:n.*3911T>G
ENST00000688985.1:c.1568T>G	ENSP00000510477.1:n.1568T>G
ENST00000689129.1:c.4492T>G	ENSP00000510414.1:p.Phe1498Val
ENST00000689177.1:n.5839T>G
ENST00000689849.1:c.663T>G
ENST00000689981.1:c.4567T>G	ENSP00000509035.1:p.Phe1523Val
ENST00000690369.1:n.4585T>G
ENST00000690590.1:n.1614T>G
ENST00000690990.1:c.4561T>G	ENSP00000510461.1:p.Phe1521Val
ENST00000691233.1:c.4486T>G	ENSP00000509215.1:p.Phe1496Val
ENST00000691306.1:c.665T>G
ENST00000691345.1:n.2302+1086T>G
ENST00000691792.1:c.4555T>G	ENSP00000509911.1:p.Phe1519Val
ENST00000691959.1:n.5286T>G
ENST00000692844.1:n.1651T>G
ENST00000692946.1:c.663T>G
ENST00000693052.1:c.4585T>G	ENSP00000509558.1:p.Phe1529Val
ENST00000693289.1:n.1726T>G
ENST00000693440.1:c.4564T>G	ENSP00000509462.1:p.Phe1522Val
ENST00000693499.1:n.5492T>G
ENST00000693591.1:n.3304T>G
ENST00000380817.8:c.4567T>G MANE Select	ENSP00000370196.2:p.Phe1523Val
ENST00000348911.10:c.4492T>G	ENSP00000252027.7:p.Phe1498Val
ENST00000380817.7:c.4567T>G	ENSP00000370196.2:p.Phe1523Val
ENST00000418590.3:c.167T>G
ENST00000470434.1:n.708T>G
NM_002972.3:c.4567T>G	NP_002963.2:p.Phe1523Val
XM_005261931.1:c.4570T>G	XP_005261988.1:p.Phe1524Val
XM_005261935.1:c.4489T>G	XP_005261992.1:p.Phe1497Val
XM_011530707.1:c.4669T>G	XP_011529009.1:p.Phe1557Val
XM_011530708.1:c.4621T>G	XP_011529010.1:p.Phe1541Val
XM_011530709.1:c.4597T>G	XP_011529011.1:p.Phe1533Val
XM_011530710.1:c.4594T>G	XP_011529012.1:p.Phe1532Val
XM_011530711.1:c.4594T>G	XP_011529013.1:p.Phe1532Val
XR_938344.1:n.4687T>G
NM_001365819.1:c.4492T>G	NP_001352748.1:p.Phe1498Val
XM_005261935.2:c.4489T>G	XP_005261992.1:p.Phe1497Val
XM_011530709.2:c.4597T>G	XP_011529011.1:p.Phe1533Val
XM_011530710.2:c.4594T>G	XP_011529012.1:p.Phe1532Val
XM_017028905.2:c.4519T>G	XP_016884394.1:p.Phe1507Val
NM_002972.4:c.4567T>G MANE Select	NP_002963.2:p.Phe1523Val