Canonical Allele Identifier: CA412193211

Gene: SBF1

Linked Data

• MyVariant Identifiers: chr22:g.50893307A>G (hg19) ; chr22:g.50454878A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50454878A>G , CM000684.2:g.50454878A>G	GRCh38
NC_000022.10:g.50893307A>G , CM000684.1:g.50893307A>G	GRCh37
NC_000022.9:g.49240173A>G	NCBI36
NG_041810.1:g.25194T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4670T>C	ENSP00000252027.8:p.Val1557Ala
ENST00000418590.4:c.380T>C	ENSP00000401538.2:p.Val127Ala
ENST00000470434.2:n.1151T>C
ENST00000684986.1:c.4751T>C	ENSP00000509117.1:p.Val1584Ala
ENST00000685180.1:n.2488+5656T>C
ENST00000685390.1:n.2716T>C
ENST00000685411.1:n.498T>C
ENST00000685592.1:c.982T>C
ENST00000685809.1:c.4661T>C	ENSP00000508863.1:p.Val1554Ala
ENST00000686029.1:c.826T>C
ENST00000686191.1:n.3948T>C
ENST00000686222.1:c.*4170T>C	ENSP00000508737.1:n.*4170T>C
ENST00000686321.1:c.844T>C
ENST00000686427.1:c.*1683T>C	ENSP00000510379.1:n.*1683T>C
ENST00000686758.1:n.2562T>C
ENST00000686801.1:c.4736T>C	ENSP00000509915.1:p.Val1579Ala
ENST00000686826.1:n.1067T>C
ENST00000687016.1:c.4649T>C	ENSP00000509074.1:p.Val1550Ala
ENST00000687704.1:c.*2473T>C	ENSP00000510454.1:n.*2473T>C
ENST00000688066.1:c.4748T>C	ENSP00000510782.1:p.Val1583Ala
ENST00000688124.1:c.*3666T>C	ENSP00000510645.1:n.*3666T>C
ENST00000688848.1:c.*4092T>C	ENSP00000509419.1:n.*4092T>C
ENST00000688985.1:c.1749T>C	ENSP00000510477.1:n.1749T>C
ENST00000689129.1:c.4673T>C	ENSP00000510414.1:p.Val1558Ala
ENST00000689177.1:n.6020T>C
ENST00000689849.1:c.844T>C
ENST00000689981.1:c.4748T>C	ENSP00000509035.1:p.Val1583Ala
ENST00000690369.1:n.4766T>C
ENST00000690590.1:n.1795T>C
ENST00000690990.1:c.4742T>C	ENSP00000510461.1:p.Val1581Ala
ENST00000691233.1:c.4667T>C	ENSP00000509215.1:p.Val1556Ala
ENST00000691306.1:c.829T>C
ENST00000691345.1:n.2302+1338T>C
ENST00000691792.1:c.4736T>C	ENSP00000509911.1:p.Val1579Ala
ENST00000691959.1:n.5467T>C
ENST00000692844.1:n.1832T>C
ENST00000692946.1:c.844T>C
ENST00000693052.1:c.4766T>C	ENSP00000509558.1:p.Val1589Ala
ENST00000693289.1:n.1907T>C
ENST00000693440.1:c.4745T>C	ENSP00000509462.1:p.Val1582Ala
ENST00000693499.1:n.5744T>C
ENST00000693591.1:n.3556T>C
ENST00000380817.8:c.4748T>C MANE Select	ENSP00000370196.2:p.Val1583Ala
ENST00000348911.10:c.4673T>C	ENSP00000252027.7:p.Val1558Ala
ENST00000380817.7:c.4748T>C	ENSP00000370196.2:p.Val1583Ala
ENST00000418590.3:c.348T>C
ENST00000470434.1:n.889T>C
NM_002972.3:c.4748T>C	NP_002963.2:p.Val1583Ala
XM_005261931.1:c.4751T>C	XP_005261988.1:p.Val1584Ala
XM_005261935.1:c.4670T>C	XP_005261992.1:p.Val1557Ala
XM_011530707.1:c.4850T>C	XP_011529009.1:p.Val1617Ala
XM_011530708.1:c.4802T>C	XP_011529010.1:p.Val1601Ala
XM_011530709.1:c.4778T>C	XP_011529011.1:p.Val1593Ala
XM_011530710.1:c.4775T>C	XP_011529012.1:p.Val1592Ala
XM_011530711.1:c.4775T>C	XP_011529013.1:p.Val1592Ala
XR_938344.1:n.4868T>C
NM_001365819.1:c.4673T>C	NP_001352748.1:p.Val1558Ala
XM_005261935.2:c.4670T>C	XP_005261992.1:p.Val1557Ala
XM_011530709.2:c.4778T>C	XP_011529011.1:p.Val1593Ala
XM_011530710.2:c.4775T>C	XP_011529012.1:p.Val1592Ala
XM_017028905.2:c.4700T>C	XP_016884394.1:p.Val1567Ala
NM_002972.4:c.4748T>C MANE Select	NP_002963.2:p.Val1583Ala