Canonical Allele Identifier: CA1951768637

Gene: SBF2 SBF2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781322_9781323delinsAG , CM000673.2:g.9781322_9781323delinsAG	GRCh38
NC_000011.9:g.9802869_9802870delinsAG , CM000673.1:g.9802869_9802870delinsAG	GRCh37
NC_000011.8:g.9759445_9759446delinsAG	NCBI36
NG_008074.1:g.517885_517886delinsCT , LRG_267:g.517885_517886delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1935+184_1935+185delinsCT (SBF2)
ENST00000675281.2:c.5526+184_5526+185delinsCT (SBF2)	ENSP00000502491.1:n.5526+184_5526+185delinsCT
ENST00000676324.2:c.*1759+184_*1759+185delinsCT (SBF2)	ENSP00000502578.1:n.*1759+184_*1759+185delinsCT
ENST00000676387.2:c.5508+184_5508+185delinsCT (SBF2)	ENSP00000502779.1:n.5508+184_5508+185delinsCT
ENST00000688344.1:c.5058+184_5058+185delinsCT (SBF2)	ENSP00000509987.1:n.5058+184_5058+185delinsCT
ENST00000689128.1:c.5547+184_5547+185delinsCT (SBF2)	ENSP00000509587.1:n.5547+184_5547+185delinsCT
ENST00000689258.1:c.5388+184_5388+185delinsCT (SBF2)	ENSP00000510475.1:n.5388+184_5388+185delinsCT
ENST00000689342.1:c.1617+184_1617+185delinsCT (SBF2)
ENST00000689356.1:n.2622+184_2622+185delinsCT (SBF2)
ENST00000689940.1:c.5445+184_5445+185delinsCT (SBF2)	ENSP00000508452.1:n.5445+184_5445+185delinsCT
ENST00000690437.1:n.1400+184_1400+185delinsCT (SBF2)
ENST00000690944.1:c.1531+184_1531+185delinsCT (SBF2)
ENST00000691616.1:n.1927+184_1927+185delinsCT (SBF2)
ENST00000692716.1:c.5322+184_5322+185delinsCT (SBF2)	ENSP00000509545.1:n.5322+184_5322+185delinsCT
ENST00000693541.1:n.2370+184_2370+185delinsCT (SBF2)
ENST00000256190.13:c.5451+184_5451+185delinsCT (SBF2) MANE Select	ENSP00000256190.8:n.5451+184_5451+185delinsCT
ENST00000675281.1:c.5526+184_5526+185delinsCT (SBF2)	ENSP00000502491.1:n.5526+184_5526+185delinsCT
ENST00000676324.1:c.*1759+184_*1759+185delinsCT (SBF2)	ENSP00000502578.1:n.*1759+184_*1759+185delinsCT
ENST00000676387.1:c.5508+184_5508+185delinsCT (SBF2)	ENSP00000502779.1:n.5508+184_5508+185delinsCT
ENST00000256190.12:c.5451+184_5451+185delinsCT (SBF2)	ENSP00000256190.8:n.5451+184_5451+185delinsCT
ENST00000525040.5:n.754+184_754+185delinsCT (SBF2)
ENST00000617179.4:c.5310+184_5310+185delinsCT (SBF2)	ENSP00000482806.1:n.5310+184_5310+185delinsCT
NM_030962.3:c.5451+184_5451+185delinsCT , LRG_267t1:c.5451+184_5451+185delinsCT (SBF2)	NP_112224.1:n.5451+184_5451+185delinsCT
NR_036485.1:n.211+22819_211+22820delinsAG (SBF2-AS1)
XM_005253154.3:c.5547+184_5547+185delinsCT (SBF2)	XP_005253211.1:n.5547+184_5547+185delinsCT
XM_005253155.3:c.5418+184_5418+185delinsCT (SBF2)	XP_005253212.1:n.5418+184_5418+185delinsCT
XM_011520394.1:c.5433+184_5433+185delinsCT (SBF2)	XP_011518696.1:n.5433+184_5433+185delinsCT
XR_931024.1:n.200+747_200+748delinsAG
XR_931025.1:n.200+747_200+748delinsAG
XM_005253154.5:c.5547+184_5547+185delinsCT (SBF2)	XP_005253211.1:n.5547+184_5547+185delinsCT
XM_005253155.5:c.5418+184_5418+185delinsCT (SBF2)	XP_005253212.1:n.5418+184_5418+185delinsCT
XM_011520394.3:c.5433+184_5433+185delinsCT (SBF2)	XP_011518696.1:n.5433+184_5433+185delinsCT
XM_017018372.2:c.5409+184_5409+185delinsCT (SBF2)	XP_016873861.1:n.5409+184_5409+185delinsCT
XM_017018373.2:c.5409+184_5409+185delinsCT (SBF2)	XP_016873862.1:n.5409+184_5409+185delinsCT
XM_017018374.2:c.5322+184_5322+185delinsCT (SBF2)	XP_016873863.1:n.5322+184_5322+185delinsCT
XM_017018375.2:c.5310+184_5310+185delinsCT (SBF2)	XP_016873864.1:n.5310+184_5310+185delinsCT
XR_001747994.2:n.5558+184_5558+185delinsCT (SBF2)
XR_001748470.1:n.200+747_200+748delinsAG
XR_001748471.1:n.85+747_85+748delinsAG
NM_001386339.1:c.5547+184_5547+185delinsCT (SBF2)	NP_001373268.1:n.5547+184_5547+185delinsCT
NM_001386342.1:c.5322+184_5322+185delinsCT (SBF2)	NP_001373271.1:n.5322+184_5322+185delinsCT
NM_030962.4:c.5451+184_5451+185delinsCT (SBF2) MANE Select	NP_112224.1:n.5451+184_5451+185delinsCT