Canonical Allele Identifier: CA2410864065

Gene: SBF1

Linked Data

• dbSNP Id: rs2067198364

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455166_50455185dup , CM000684.2:g.50455166_50455185dup	GRCh38
NC_000022.10:g.50893595_50893614dup , CM000684.1:g.50893595_50893614dup	GRCh37
NC_000022.9:g.49240461_49240480dup	NCBI36
NG_041810.1:g.24890_24909dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4477-40_4477-21dup	ENSP00000252027.8:n.4477-40_4477-21dup
ENST00000418590.4:c.187-40_187-21dup	ENSP00000401538.2:n.187-40_187-21dup
ENST00000470434.2:n.918_937dup
ENST00000684986.1:c.4558-40_4558-21dup	ENSP00000509117.1:n.4558-40_4558-21dup
ENST00000685180.1:n.2488+5352_2488+5371dup
ENST00000685390.1:n.2523-40_2523-21dup
ENST00000685411.1:n.265_284dup
ENST00000685592.1:c.789-40_789-21dup
ENST00000685809.1:c.4468-40_4468-21dup	ENSP00000508863.1:n.4468-40_4468-21dup
ENST00000686029.1:c.633-40_633-21dup
ENST00000686191.1:n.3755-40_3755-21dup
ENST00000686222.1:c.*3977-40_*3977-21dup	ENSP00000508737.1:n.*3977-40_*3977-21dup
ENST00000686321.1:c.651-40_651-21dup
ENST00000686427.1:c.*1490-40_*1490-21dup	ENSP00000510379.1:n.*1490-40_*1490-21dup
ENST00000686758.1:n.2258_2277dup
ENST00000686801.1:c.4543-40_4543-21dup	ENSP00000509915.1:n.4543-40_4543-21dup
ENST00000686826.1:n.874-40_874-21dup
ENST00000687016.1:c.4456-40_4456-21dup	ENSP00000509074.1:n.4456-40_4456-21dup
ENST00000687704.1:c.*2280-40_*2280-21dup	ENSP00000510454.1:n.*2280-40_*2280-21dup
ENST00000688066.1:c.4555-40_4555-21dup	ENSP00000510782.1:n.4555-40_4555-21dup
ENST00000688124.1:c.*3473-40_*3473-21dup	ENSP00000510645.1:n.*3473-40_*3473-21dup
ENST00000688848.1:c.*3899-40_*3899-21dup	ENSP00000509419.1:n.*3899-40_*3899-21dup
ENST00000688985.1:c.1556-40_1556-21dup	ENSP00000510477.1:n.1556-40_1556-21dup
ENST00000689129.1:c.4480-40_4480-21dup	ENSP00000510414.1:n.4480-40_4480-21dup
ENST00000689177.1:n.5827-40_5827-21dup
ENST00000689849.1:c.651-40_651-21dup
ENST00000689981.1:c.4555-40_4555-21dup	ENSP00000509035.1:n.4555-40_4555-21dup
ENST00000690369.1:n.4573-40_4573-21dup
ENST00000690590.1:n.1602-40_1602-21dup
ENST00000690990.1:c.4549-40_4549-21dup	ENSP00000510461.1:n.4549-40_4549-21dup
ENST00000691233.1:c.4474-40_4474-21dup	ENSP00000509215.1:n.4474-40_4474-21dup
ENST00000691306.1:c.653-40_653-21dup
ENST00000691345.1:n.2302+1034_2302+1053dup
ENST00000691792.1:c.4554+42_4555-33dup	ENSP00000509911.1:n.4554+42_4555-33dup
ENST00000691959.1:n.5274-40_5274-21dup
ENST00000692844.1:n.1639-40_1639-21dup
ENST00000692946.1:c.651-40_651-21dup
ENST00000693052.1:c.4573-40_4573-21dup	ENSP00000509558.1:n.4573-40_4573-21dup
ENST00000693289.1:n.1714-40_1714-21dup
ENST00000693440.1:c.4552-40_4552-21dup	ENSP00000509462.1:n.4552-40_4552-21dup
ENST00000693499.1:n.5480-40_5480-21dup
ENST00000693591.1:n.3292-40_3292-21dup
ENST00000380817.8:c.4555-40_4555-21dup MANE Select	ENSP00000370196.2:n.4555-40_4555-21dup
ENST00000348911.10:c.4480-40_4480-21dup	ENSP00000252027.7:n.4480-40_4480-21dup
ENST00000380817.7:c.4555-40_4555-21dup	ENSP00000370196.2:n.4555-40_4555-21dup
ENST00000418590.3:c.155-40_155-21dup
ENST00000470434.1:n.696-40_696-21dup
NM_002972.3:c.4555-40_4555-21dup	NP_002963.2:n.4555-40_4555-21dup
XM_005261931.1:c.4558-40_4558-21dup	XP_005261988.1:n.4558-40_4558-21dup
XM_005261935.1:c.4477-40_4477-21dup	XP_005261992.1:n.4477-40_4477-21dup
XM_011530707.1:c.4657-40_4657-21dup	XP_011529009.1:n.4657-40_4657-21dup
XM_011530708.1:c.4609-40_4609-21dup	XP_011529010.1:n.4609-40_4609-21dup
XM_011530709.1:c.4585-40_4585-21dup	XP_011529011.1:n.4585-40_4585-21dup
XM_011530710.1:c.4582-40_4582-21dup	XP_011529012.1:n.4582-40_4582-21dup
XM_011530711.1:c.4582-40_4582-21dup	XP_011529013.1:n.4582-40_4582-21dup
XR_938344.1:n.4675-40_4675-21dup
NM_001365819.1:c.4480-40_4480-21dup	NP_001352748.1:n.4480-40_4480-21dup
XM_005261935.2:c.4477-40_4477-21dup	XP_005261992.1:n.4477-40_4477-21dup
XM_011530709.2:c.4585-40_4585-21dup	XP_011529011.1:n.4585-40_4585-21dup
XM_011530710.2:c.4582-40_4582-21dup	XP_011529012.1:n.4582-40_4582-21dup
XM_017028905.2:c.4507-40_4507-21dup	XP_016884394.1:n.4507-40_4507-21dup
NM_002972.4:c.4555-40_4555-21dup MANE Select	NP_002963.2:n.4555-40_4555-21dup