Canonical Allele Identifier: CA412195357

Gene: SBF1

Linked Data

• MyVariant Identifiers: chr22:g.50893546A>G (hg19) ; chr22:g.50455117A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455117A>G , CM000684.2:g.50455117A>G	GRCh38
NC_000022.10:g.50893546A>G , CM000684.1:g.50893546A>G	GRCh37
NC_000022.9:g.49240412A>G	NCBI36
NG_041810.1:g.24955T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4502T>C	ENSP00000252027.8:p.Phe1501Ser
ENST00000418590.4:c.212T>C	ENSP00000401538.2:p.Phe71Ser
ENST00000470434.2:n.983T>C
ENST00000684986.1:c.4583T>C	ENSP00000509117.1:p.Phe1528Ser
ENST00000685180.1:n.2488+5417T>C
ENST00000685390.1:n.2548T>C
ENST00000685411.1:n.330T>C
ENST00000685592.1:c.814T>C
ENST00000685809.1:c.4493T>C	ENSP00000508863.1:p.Phe1498Ser
ENST00000686029.1:c.658T>C
ENST00000686191.1:n.3780T>C
ENST00000686222.1:c.*4002T>C	ENSP00000508737.1:n.*4002T>C
ENST00000686321.1:c.676T>C
ENST00000686427.1:c.*1515T>C	ENSP00000510379.1:n.*1515T>C
ENST00000686758.1:n.2323T>C
ENST00000686801.1:c.4568T>C	ENSP00000509915.1:p.Phe1523Ser
ENST00000686826.1:n.899T>C
ENST00000687016.1:c.4481T>C	ENSP00000509074.1:p.Phe1494Ser
ENST00000687704.1:c.*2305T>C	ENSP00000510454.1:n.*2305T>C
ENST00000688066.1:c.4580T>C	ENSP00000510782.1:p.Phe1527Ser
ENST00000688124.1:c.*3498T>C	ENSP00000510645.1:n.*3498T>C
ENST00000688848.1:c.*3924T>C	ENSP00000509419.1:n.*3924T>C
ENST00000688985.1:c.1581T>C	ENSP00000510477.1:n.1581T>C
ENST00000689129.1:c.4505T>C	ENSP00000510414.1:p.Phe1502Ser
ENST00000689177.1:n.5852T>C
ENST00000689849.1:c.676T>C
ENST00000689981.1:c.4580T>C	ENSP00000509035.1:p.Phe1527Ser
ENST00000690369.1:n.4598T>C
ENST00000690590.1:n.1627T>C
ENST00000690990.1:c.4574T>C	ENSP00000510461.1:p.Phe1525Ser
ENST00000691233.1:c.4499T>C	ENSP00000509215.1:p.Phe1500Ser
ENST00000691306.1:c.678T>C
ENST00000691345.1:n.2302+1099T>C
ENST00000691792.1:c.4568T>C	ENSP00000509911.1:p.Phe1523Ser
ENST00000691959.1:n.5299T>C
ENST00000692844.1:n.1664T>C
ENST00000692946.1:c.676T>C
ENST00000693052.1:c.4598T>C	ENSP00000509558.1:p.Phe1533Ser
ENST00000693289.1:n.1739T>C
ENST00000693440.1:c.4577T>C	ENSP00000509462.1:p.Phe1526Ser
ENST00000693499.1:n.5505T>C
ENST00000693591.1:n.3317T>C
ENST00000380817.8:c.4580T>C MANE Select	ENSP00000370196.2:p.Phe1527Ser
ENST00000348911.10:c.4505T>C	ENSP00000252027.7:p.Phe1502Ser
ENST00000380817.7:c.4580T>C	ENSP00000370196.2:p.Phe1527Ser
ENST00000418590.3:c.180T>C
ENST00000470434.1:n.721T>C
NM_002972.3:c.4580T>C	NP_002963.2:p.Phe1527Ser
XM_005261931.1:c.4583T>C	XP_005261988.1:p.Phe1528Ser
XM_005261935.1:c.4502T>C	XP_005261992.1:p.Phe1501Ser
XM_011530707.1:c.4682T>C	XP_011529009.1:p.Phe1561Ser
XM_011530708.1:c.4634T>C	XP_011529010.1:p.Phe1545Ser
XM_011530709.1:c.4610T>C	XP_011529011.1:p.Phe1537Ser
XM_011530710.1:c.4607T>C	XP_011529012.1:p.Phe1536Ser
XM_011530711.1:c.4607T>C	XP_011529013.1:p.Phe1536Ser
XR_938344.1:n.4700T>C
NM_001365819.1:c.4505T>C	NP_001352748.1:p.Phe1502Ser
XM_005261935.2:c.4502T>C	XP_005261992.1:p.Phe1501Ser
XM_011530709.2:c.4610T>C	XP_011529011.1:p.Phe1537Ser
XM_011530710.2:c.4607T>C	XP_011529012.1:p.Phe1536Ser
XM_017028905.2:c.4532T>C	XP_016884394.1:p.Phe1511Ser
NM_002972.4:c.4580T>C MANE Select	NP_002963.2:p.Phe1527Ser