Canonical Allele Identifier: CA1951768856
Gene: SBF2 HGNC NCBI
SBF2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9781449_9781453delinsGAGAC , CM000673.2:g.9781449_9781453delinsGAGAC GRCh38
NC_000011.9:g.9802996_9803000delinsGAGAC , CM000673.1:g.9802996_9803000delinsGAGAC GRCh37
NC_000011.8:g.9759572_9759576delinsGAGAC NCBI36
NG_008074.1:g.517755_517759delinsGTCTC , LRG_267:g.517755_517759delinsGTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000524961.6:n.1935+54_1935+58delinsGTCTC (SBF2)
ENST00000675281.2:c.5526+54_5526+58delinsGTCTC (SBF2) ENSP00000502491.1:n.5526+54_5526+58delinsGTCTC
ENST00000676324.2:c.*1759+54_*1759+58delinsGTCTC (SBF2) ENSP00000502578.1:n.*1759+54_*1759+58delinsGTCTC
ENST00000676387.2:c.5508+54_5508+58delinsGTCTC (SBF2) ENSP00000502779.1:n.5508+54_5508+58delinsGTCTC
ENST00000688344.1:c.5058+54_5058+58delinsGTCTC (SBF2) ENSP00000509987.1:n.5058+54_5058+58delinsGTCTC
ENST00000689128.1:c.5547+54_5547+58delinsGTCTC (SBF2) ENSP00000509587.1:n.5547+54_5547+58delinsGTCTC
ENST00000689258.1:c.5388+54_5388+58delinsGTCTC (SBF2) ENSP00000510475.1:n.5388+54_5388+58delinsGTCTC
ENST00000689342.1:c.1617+54_1617+58delinsGTCTC (SBF2)
ENST00000689356.1:n.2622+54_2622+58delinsGTCTC (SBF2)
ENST00000689940.1:c.5445+54_5445+58delinsGTCTC (SBF2) ENSP00000508452.1:n.5445+54_5445+58delinsGTCTC
ENST00000690437.1:n.1400+54_1400+58delinsGTCTC (SBF2)
ENST00000690944.1:c.1531+54_1531+58delinsGTCTC (SBF2)
ENST00000691616.1:n.1927+54_1927+58delinsGTCTC (SBF2)
ENST00000692716.1:c.5322+54_5322+58delinsGTCTC (SBF2) ENSP00000509545.1:n.5322+54_5322+58delinsGTCTC
ENST00000693541.1:n.2370+54_2370+58delinsGTCTC (SBF2)
ENST00000256190.13:c.5451+54_5451+58delinsGTCTC (SBF2) MANE Select ENSP00000256190.8:n.5451+54_5451+58delinsGTCTC
ENST00000675281.1:c.5526+54_5526+58delinsGTCTC (SBF2) ENSP00000502491.1:n.5526+54_5526+58delinsGTCTC
ENST00000676324.1:c.*1759+54_*1759+58delinsGTCTC (SBF2) ENSP00000502578.1:n.*1759+54_*1759+58delinsGTCTC
ENST00000676387.1:c.5508+54_5508+58delinsGTCTC (SBF2) ENSP00000502779.1:n.5508+54_5508+58delinsGTCTC
ENST00000256190.12:c.5451+54_5451+58delinsGTCTC (SBF2) ENSP00000256190.8:n.5451+54_5451+58delinsGTCTC
ENST00000525040.5:n.754+54_754+58delinsGTCTC (SBF2)
ENST00000617179.4:c.5310+54_5310+58delinsGTCTC (SBF2) ENSP00000482806.1:n.5310+54_5310+58delinsGTCTC
NM_030962.3:c.5451+54_5451+58delinsGTCTC , LRG_267t1:c.5451+54_5451+58delinsGTCTC (SBF2) NP_112224.1:n.5451+54_5451+58delinsGTCTC
NR_036485.1:n.211+22946_211+22950delinsGAGAC (SBF2-AS1)
XM_005253154.3:c.5547+54_5547+58delinsGTCTC (SBF2) XP_005253211.1:n.5547+54_5547+58delinsGTCTC
XM_005253155.3:c.5418+54_5418+58delinsGTCTC (SBF2) XP_005253212.1:n.5418+54_5418+58delinsGTCTC
XM_011520394.1:c.5433+54_5433+58delinsGTCTC (SBF2) XP_011518696.1:n.5433+54_5433+58delinsGTCTC
XR_931024.1:n.200+874_200+878delinsGAGAC
XR_931025.1:n.200+874_200+878delinsGAGAC
XM_005253154.5:c.5547+54_5547+58delinsGTCTC (SBF2) XP_005253211.1:n.5547+54_5547+58delinsGTCTC
XM_005253155.5:c.5418+54_5418+58delinsGTCTC (SBF2) XP_005253212.1:n.5418+54_5418+58delinsGTCTC
XM_011520394.3:c.5433+54_5433+58delinsGTCTC (SBF2) XP_011518696.1:n.5433+54_5433+58delinsGTCTC
XM_017018372.2:c.5409+54_5409+58delinsGTCTC (SBF2) XP_016873861.1:n.5409+54_5409+58delinsGTCTC
XM_017018373.2:c.5409+54_5409+58delinsGTCTC (SBF2) XP_016873862.1:n.5409+54_5409+58delinsGTCTC
XM_017018374.2:c.5322+54_5322+58delinsGTCTC (SBF2) XP_016873863.1:n.5322+54_5322+58delinsGTCTC
XM_017018375.2:c.5310+54_5310+58delinsGTCTC (SBF2) XP_016873864.1:n.5310+54_5310+58delinsGTCTC
XR_001747994.2:n.5558+54_5558+58delinsGTCTC (SBF2)
XR_001748470.1:n.200+874_200+878delinsGAGAC
XR_001748471.1:n.85+874_85+878delinsGAGAC
NM_001386339.1:c.5547+54_5547+58delinsGTCTC (SBF2) NP_001373268.1:n.5547+54_5547+58delinsGTCTC
NM_001386342.1:c.5322+54_5322+58delinsGTCTC (SBF2) NP_001373271.1:n.5322+54_5322+58delinsGTCTC
NM_030962.4:c.5451+54_5451+58delinsGTCTC (SBF2) MANE Select NP_112224.1:n.5451+54_5451+58delinsGTCTC