Canonical Allele Identifier: CA2580617756

Gene: SBF1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455003A>C , CM000684.2:g.50455003A>C	GRCh38
NC_000022.10:g.50893432A>C , CM000684.1:g.50893432A>C	GRCh37
NC_000022.9:g.49240298A>C	NCBI36
NG_041810.1:g.25069T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4603+13T>G	ENSP00000252027.8:n.4603+13T>G
ENST00000418590.4:c.313+13T>G	ENSP00000401538.2:n.313+13T>G
ENST00000470434.2:n.1084+13T>G
ENST00000684986.1:c.4684+13T>G	ENSP00000509117.1:n.4684+13T>G
ENST00000685180.1:n.2488+5531T>G
ENST00000685390.1:n.2649+13T>G
ENST00000685411.1:n.431+13T>G
ENST00000685592.1:c.915+13T>G
ENST00000685809.1:c.4594+13T>G	ENSP00000508863.1:n.4594+13T>G
ENST00000686029.1:c.759+13T>G
ENST00000686191.1:n.3881+13T>G
ENST00000686222.1:c.*4103+13T>G	ENSP00000508737.1:n.*4103+13T>G
ENST00000686321.1:c.777+13T>G
ENST00000686427.1:c.*1616+13T>G	ENSP00000510379.1:n.*1616+13T>G
ENST00000686758.1:n.2437T>G
ENST00000686801.1:c.4669+13T>G	ENSP00000509915.1:n.4669+13T>G
ENST00000686826.1:n.1000+13T>G
ENST00000687016.1:c.4582+13T>G	ENSP00000509074.1:n.4582+13T>G
ENST00000687704.1:c.*2406+13T>G	ENSP00000510454.1:n.*2406+13T>G
ENST00000688066.1:c.4681+13T>G	ENSP00000510782.1:n.4681+13T>G
ENST00000688124.1:c.*3599+13T>G	ENSP00000510645.1:n.*3599+13T>G
ENST00000688848.1:c.*4025+13T>G	ENSP00000509419.1:n.*4025+13T>G
ENST00000688985.1:c.1682+13T>G	ENSP00000510477.1:n.1682+13T>G
ENST00000689129.1:c.4606+13T>G	ENSP00000510414.1:n.4606+13T>G
ENST00000689177.1:n.5953+13T>G
ENST00000689849.1:c.777+13T>G
ENST00000689981.1:c.4681+13T>G	ENSP00000509035.1:n.4681+13T>G
ENST00000690369.1:n.4699+13T>G
ENST00000690590.1:n.1728+13T>G
ENST00000690990.1:c.4675+13T>G	ENSP00000510461.1:n.4675+13T>G
ENST00000691233.1:c.4600+13T>G	ENSP00000509215.1:n.4600+13T>G
ENST00000691306.1:c.779+13T>G
ENST00000691345.1:n.2302+1213T>G
ENST00000691792.1:c.4669+13T>G	ENSP00000509911.1:n.4669+13T>G
ENST00000691959.1:n.5400+13T>G
ENST00000692844.1:n.1765+13T>G
ENST00000692946.1:c.777+13T>G
ENST00000693052.1:c.4699+13T>G	ENSP00000509558.1:n.4699+13T>G
ENST00000693289.1:n.1840+13T>G
ENST00000693440.1:c.4678+13T>G	ENSP00000509462.1:n.4678+13T>G
ENST00000693499.1:n.5619T>G
ENST00000693591.1:n.3431T>G
ENST00000380817.8:c.4681+13T>G MANE Select	ENSP00000370196.2:n.4681+13T>G
ENST00000348911.10:c.4606+13T>G	ENSP00000252027.7:n.4606+13T>G
ENST00000380817.7:c.4681+13T>G	ENSP00000370196.2:n.4681+13T>G
ENST00000418590.3:c.281+13T>G
ENST00000470434.1:n.822+13T>G
NM_002972.3:c.4681+13T>G	NP_002963.2:n.4681+13T>G
XM_005261931.1:c.4684+13T>G	XP_005261988.1:n.4684+13T>G
XM_005261935.1:c.4603+13T>G	XP_005261992.1:n.4603+13T>G
XM_011530707.1:c.4783+13T>G	XP_011529009.1:n.4783+13T>G
XM_011530708.1:c.4735+13T>G	XP_011529010.1:n.4735+13T>G
XM_011530709.1:c.4711+13T>G	XP_011529011.1:n.4711+13T>G
XM_011530710.1:c.4708+13T>G	XP_011529012.1:n.4708+13T>G
XM_011530711.1:c.4708+13T>G	XP_011529013.1:n.4708+13T>G
XR_938344.1:n.4801+13T>G
NM_001365819.1:c.4606+13T>G	NP_001352748.1:n.4606+13T>G
XM_005261935.2:c.4603+13T>G	XP_005261992.1:n.4603+13T>G
XM_011530709.2:c.4711+13T>G	XP_011529011.1:n.4711+13T>G
XM_011530710.2:c.4708+13T>G	XP_011529012.1:n.4708+13T>G
XM_017028905.2:c.4633+13T>G	XP_016884394.1:n.4633+13T>G
NM_002972.4:c.4681+13T>G MANE Select	NP_002963.2:n.4681+13T>G