Canonical Allele Identifier: CA325528047

Gene: SBF1

Linked Data

• dbSNP Id: rs376756811
• MyVariant Identifiers: chr22:g.50893412_50893413insA (hg19) ; chr22:g.50454983_50454984insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50454983_50454984insA , CM000684.2:g.50454983_50454984insA	GRCh38
NC_000022.10:g.50893412_50893413insA , CM000684.1:g.50893412_50893413insA	GRCh37
NC_000022.9:g.49240278_49240279insA	NCBI36
NG_041810.1:g.25088_25089insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4603+32_4603+33insT	ENSP00000252027.8:n.4603+32_4603+33insT
ENST00000418590.4:c.313+32_313+33insT	ENSP00000401538.2:n.313+32_313+33insT
ENST00000470434.2:n.1084+32_1084+33insT
ENST00000684986.1:c.4684+32_4684+33insT	ENSP00000509117.1:n.4684+32_4684+33insT
ENST00000685180.1:n.2488+5550_2488+5551insT
ENST00000685390.1:n.2649+32_2649+33insT
ENST00000685411.1:n.431+32_431+33insT
ENST00000685592.1:c.915+32_915+33insT
ENST00000685809.1:c.4594+32_4594+33insT	ENSP00000508863.1:n.4594+32_4594+33insT
ENST00000686029.1:c.759+32_759+33insT
ENST00000686191.1:n.3881+32_3881+33insT
ENST00000686222.1:c.*4103+32_*4103+33insT	ENSP00000508737.1:n.*4103+32_*4103+33insT
ENST00000686321.1:c.777+32_777+33insT
ENST00000686427.1:c.*1616+32_*1616+33insT	ENSP00000510379.1:n.*1616+32_*1616+33insT
ENST00000686758.1:n.2456_2457insT
ENST00000686801.1:c.4669+32_4669+33insT	ENSP00000509915.1:n.4669+32_4669+33insT
ENST00000686826.1:n.1000+32_1000+33insT
ENST00000687016.1:c.4582+32_4582+33insT	ENSP00000509074.1:n.4582+32_4582+33insT
ENST00000687704.1:c.*2406+32_*2406+33insT	ENSP00000510454.1:n.*2406+32_*2406+33insT
ENST00000688066.1:c.4681+32_4681+33insT	ENSP00000510782.1:n.4681+32_4681+33insT
ENST00000688124.1:c.*3599+32_*3599+33insT	ENSP00000510645.1:n.*3599+32_*3599+33insT
ENST00000688848.1:c.*4025+32_*4025+33insT	ENSP00000509419.1:n.*4025+32_*4025+33insT
ENST00000688985.1:c.1682+32_1682+33insT	ENSP00000510477.1:n.1682+32_1682+33insT
ENST00000689129.1:c.4606+32_4606+33insT	ENSP00000510414.1:n.4606+32_4606+33insT
ENST00000689177.1:n.5953+32_5953+33insT
ENST00000689849.1:c.777+32_777+33insT
ENST00000689981.1:c.4681+32_4681+33insT	ENSP00000509035.1:n.4681+32_4681+33insT
ENST00000690369.1:n.4699+32_4699+33insT
ENST00000690590.1:n.1728+32_1728+33insT
ENST00000690990.1:c.4675+32_4675+33insT	ENSP00000510461.1:n.4675+32_4675+33insT
ENST00000691233.1:c.4600+32_4600+33insT	ENSP00000509215.1:n.4600+32_4600+33insT
ENST00000691306.1:c.779+32_779+33insT
ENST00000691345.1:n.2302+1232_2302+1233insT
ENST00000691792.1:c.4669+32_4669+33insT	ENSP00000509911.1:n.4669+32_4669+33insT
ENST00000691959.1:n.5400+32_5400+33insT
ENST00000692844.1:n.1765+32_1765+33insT
ENST00000692946.1:c.777+32_777+33insT
ENST00000693052.1:c.4699+32_4699+33insT	ENSP00000509558.1:n.4699+32_4699+33insT
ENST00000693289.1:n.1840+32_1840+33insT
ENST00000693440.1:c.4678+32_4678+33insT	ENSP00000509462.1:n.4678+32_4678+33insT
ENST00000693499.1:n.5638_5639insT
ENST00000693591.1:n.3450_3451insT
ENST00000380817.8:c.4681+32_4681+33insT MANE Select	ENSP00000370196.2:n.4681+32_4681+33insT
ENST00000348911.10:c.4606+32_4606+33insT	ENSP00000252027.7:n.4606+32_4606+33insT
ENST00000380817.7:c.4681+32_4681+33insT	ENSP00000370196.2:n.4681+32_4681+33insT
ENST00000418590.3:c.281+32_281+33insT
ENST00000470434.1:n.822+32_822+33insT
NM_002972.3:c.4681+32_4681+33insT	NP_002963.2:n.4681+32_4681+33insT
XM_005261931.1:c.4684+32_4684+33insT	XP_005261988.1:n.4684+32_4684+33insT
XM_005261935.1:c.4603+32_4603+33insT	XP_005261992.1:n.4603+32_4603+33insT
XM_011530707.1:c.4783+32_4783+33insT	XP_011529009.1:n.4783+32_4783+33insT
XM_011530708.1:c.4735+32_4735+33insT	XP_011529010.1:n.4735+32_4735+33insT
XM_011530709.1:c.4711+32_4711+33insT	XP_011529011.1:n.4711+32_4711+33insT
XM_011530710.1:c.4708+32_4708+33insT	XP_011529012.1:n.4708+32_4708+33insT
XM_011530711.1:c.4708+32_4708+33insT	XP_011529013.1:n.4708+32_4708+33insT
XR_938344.1:n.4801+32_4801+33insT
NM_001365819.1:c.4606+32_4606+33insT	NP_001352748.1:n.4606+32_4606+33insT
XM_005261935.2:c.4603+32_4603+33insT	XP_005261992.1:n.4603+32_4603+33insT
XM_011530709.2:c.4711+32_4711+33insT	XP_011529011.1:n.4711+32_4711+33insT
XM_011530710.2:c.4708+32_4708+33insT	XP_011529012.1:n.4708+32_4708+33insT
XM_017028905.2:c.4633+32_4633+33insT	XP_016884394.1:n.4633+32_4633+33insT
NM_002972.4:c.4681+32_4681+33insT MANE Select	NP_002963.2:n.4681+32_4681+33insT