Canonical Allele Identifier: CA597552397

Gene: SBF2 SBF2-AS1

Linked Data

• dbSNP Id: rs1217906756
• gnomAD v2: 11-9802654-A-ATGTT
• gnomAD v3: 11-9781107-A-ATGTT
• gnomAD v4: 11-9781107-A-ATGTT
• MyVariant Identifiers: chr11:g.9802654_9802655insTGTT (hg19) ; chr11:g.9781107_9781108insTGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781108_9781111dup , CM000673.2:g.9781108_9781111dup	GRCh38
NC_000011.9:g.9802655_9802658dup , CM000673.1:g.9802655_9802658dup	GRCh37
NC_000011.8:g.9759231_9759234dup	NCBI36
NG_008074.1:g.518097_518100dup , LRG_267:g.518097_518100dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1935+396_1935+399dup (SBF2)
ENST00000675281.2:c.5526+396_5526+399dup (SBF2)	ENSP00000502491.1:n.5526+396_5526+399dup
ENST00000676324.2:c.*1759+396_*1759+399dup (SBF2)	ENSP00000502578.1:n.*1759+396_*1759+399dup
ENST00000676387.2:c.5508+396_5508+399dup (SBF2)	ENSP00000502779.1:n.5508+396_5508+399dup
ENST00000688344.1:c.5058+396_5058+399dup (SBF2)	ENSP00000509987.1:n.5058+396_5058+399dup
ENST00000689128.1:c.5547+396_5547+399dup (SBF2)	ENSP00000509587.1:n.5547+396_5547+399dup
ENST00000689258.1:c.5388+396_5388+399dup (SBF2)	ENSP00000510475.1:n.5388+396_5388+399dup
ENST00000689342.1:c.1617+396_1617+399dup (SBF2)
ENST00000689356.1:n.2622+396_2622+399dup (SBF2)
ENST00000689940.1:c.5445+396_5445+399dup (SBF2)	ENSP00000508452.1:n.5445+396_5445+399dup
ENST00000690437.1:n.1400+396_1400+399dup (SBF2)
ENST00000690944.1:c.1531+396_1531+399dup (SBF2)
ENST00000691616.1:n.1927+396_1927+399dup (SBF2)
ENST00000692716.1:c.5322+396_5322+399dup (SBF2)	ENSP00000509545.1:n.5322+396_5322+399dup
ENST00000693541.1:n.2370+396_2370+399dup (SBF2)
ENST00000256190.13:c.5451+396_5451+399dup (SBF2) MANE Select	ENSP00000256190.8:n.5451+396_5451+399dup
ENST00000675281.1:c.5526+396_5526+399dup (SBF2)	ENSP00000502491.1:n.5526+396_5526+399dup
ENST00000676324.1:c.*1759+396_*1759+399dup (SBF2)	ENSP00000502578.1:n.*1759+396_*1759+399dup
ENST00000676387.1:c.5508+396_5508+399dup (SBF2)	ENSP00000502779.1:n.5508+396_5508+399dup
ENST00000256190.12:c.5451+396_5451+399dup (SBF2)	ENSP00000256190.8:n.5451+396_5451+399dup
ENST00000525040.5:n.754+396_754+399dup (SBF2)
ENST00000617179.4:c.5310+396_5310+399dup (SBF2)	ENSP00000482806.1:n.5310+396_5310+399dup
NM_030962.3:c.5451+396_5451+399dup , LRG_267t1:c.5451+396_5451+399dup (SBF2)	NP_112224.1:n.5451+396_5451+399dup
NR_036485.1:n.211+22605_211+22608dup (SBF2-AS1)
XM_005253154.3:c.5547+396_5547+399dup (SBF2)	XP_005253211.1:n.5547+396_5547+399dup
XM_005253155.3:c.5418+396_5418+399dup (SBF2)	XP_005253212.1:n.5418+396_5418+399dup
XM_011520394.1:c.5433+396_5433+399dup (SBF2)	XP_011518696.1:n.5433+396_5433+399dup
XR_931024.1:n.200+533_200+536dup
XR_931025.1:n.200+533_200+536dup
XM_005253154.5:c.5547+396_5547+399dup (SBF2)	XP_005253211.1:n.5547+396_5547+399dup
XM_005253155.5:c.5418+396_5418+399dup (SBF2)	XP_005253212.1:n.5418+396_5418+399dup
XM_011520394.3:c.5433+396_5433+399dup (SBF2)	XP_011518696.1:n.5433+396_5433+399dup
XM_017018372.2:c.5409+396_5409+399dup (SBF2)	XP_016873861.1:n.5409+396_5409+399dup
XM_017018373.2:c.5409+396_5409+399dup (SBF2)	XP_016873862.1:n.5409+396_5409+399dup
XM_017018374.2:c.5322+396_5322+399dup (SBF2)	XP_016873863.1:n.5322+396_5322+399dup
XM_017018375.2:c.5310+396_5310+399dup (SBF2)	XP_016873864.1:n.5310+396_5310+399dup
XR_001747994.2:n.5558+396_5558+399dup (SBF2)
XR_001748470.1:n.200+533_200+536dup
XR_001748471.1:n.85+533_85+536dup
NM_001386339.1:c.5547+396_5547+399dup (SBF2)	NP_001373268.1:n.5547+396_5547+399dup
NM_001386342.1:c.5322+396_5322+399dup (SBF2)	NP_001373271.1:n.5322+396_5322+399dup
NM_030962.4:c.5451+396_5451+399dup (SBF2) MANE Select	NP_112224.1:n.5451+396_5451+399dup