Canonical Allele Identifier: CA1951768842

Gene: SBF2 SBF2-AS1

Linked Data

• dbSNP Id: rs1851999068
• gnomAD v4: 11-9781437-CCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781441_9781443del , CM000673.2:g.9781441_9781443del	GRCh38
NC_000011.9:g.9802988_9802990del , CM000673.1:g.9802988_9802990del	GRCh37
NC_000011.8:g.9759564_9759566del	NCBI36
NG_008074.1:g.517768_517770del , LRG_267:g.517768_517770del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1935+67_1935+69del (SBF2)
ENST00000675281.2:c.5526+67_5526+69del (SBF2)	ENSP00000502491.1:n.5526+67_5526+69del
ENST00000676324.2:c.*1759+67_*1759+69del (SBF2)	ENSP00000502578.1:n.*1759+67_*1759+69del
ENST00000676387.2:c.5508+67_5508+69del (SBF2)	ENSP00000502779.1:n.5508+67_5508+69del
ENST00000688344.1:c.5058+67_5058+69del (SBF2)	ENSP00000509987.1:n.5058+67_5058+69del
ENST00000689128.1:c.5547+67_5547+69del (SBF2)	ENSP00000509587.1:n.5547+67_5547+69del
ENST00000689258.1:c.5388+67_5388+69del (SBF2)	ENSP00000510475.1:n.5388+67_5388+69del
ENST00000689342.1:c.1617+67_1617+69del (SBF2)
ENST00000689356.1:n.2622+67_2622+69del (SBF2)
ENST00000689940.1:c.5445+67_5445+69del (SBF2)	ENSP00000508452.1:n.5445+67_5445+69del
ENST00000690437.1:n.1400+67_1400+69del (SBF2)
ENST00000690944.1:c.1531+67_1531+69del (SBF2)
ENST00000691616.1:n.1927+67_1927+69del (SBF2)
ENST00000692716.1:c.5322+67_5322+69del (SBF2)	ENSP00000509545.1:n.5322+67_5322+69del
ENST00000693541.1:n.2370+67_2370+69del (SBF2)
ENST00000256190.13:c.5451+67_5451+69del (SBF2) MANE Select	ENSP00000256190.8:n.5451+67_5451+69del
ENST00000675281.1:c.5526+67_5526+69del (SBF2)	ENSP00000502491.1:n.5526+67_5526+69del
ENST00000676324.1:c.*1759+67_*1759+69del (SBF2)	ENSP00000502578.1:n.*1759+67_*1759+69del
ENST00000676387.1:c.5508+67_5508+69del (SBF2)	ENSP00000502779.1:n.5508+67_5508+69del
ENST00000256190.12:c.5451+67_5451+69del (SBF2)	ENSP00000256190.8:n.5451+67_5451+69del
ENST00000525040.5:n.754+67_754+69del (SBF2)
ENST00000617179.4:c.5310+67_5310+69del (SBF2)	ENSP00000482806.1:n.5310+67_5310+69del
NM_030962.3:c.5451+67_5451+69del , LRG_267t1:c.5451+67_5451+69del (SBF2)	NP_112224.1:n.5451+67_5451+69del
NR_036485.1:n.211+22938_211+22940del (SBF2-AS1)
XM_005253154.3:c.5547+67_5547+69del (SBF2)	XP_005253211.1:n.5547+67_5547+69del
XM_005253155.3:c.5418+67_5418+69del (SBF2)	XP_005253212.1:n.5418+67_5418+69del
XM_011520394.1:c.5433+67_5433+69del (SBF2)	XP_011518696.1:n.5433+67_5433+69del
XR_931024.1:n.200+866_200+868del
XR_931025.1:n.200+866_200+868del
XM_005253154.5:c.5547+67_5547+69del (SBF2)	XP_005253211.1:n.5547+67_5547+69del
XM_005253155.5:c.5418+67_5418+69del (SBF2)	XP_005253212.1:n.5418+67_5418+69del
XM_011520394.3:c.5433+67_5433+69del (SBF2)	XP_011518696.1:n.5433+67_5433+69del
XM_017018372.2:c.5409+67_5409+69del (SBF2)	XP_016873861.1:n.5409+67_5409+69del
XM_017018373.2:c.5409+67_5409+69del (SBF2)	XP_016873862.1:n.5409+67_5409+69del
XM_017018374.2:c.5322+67_5322+69del (SBF2)	XP_016873863.1:n.5322+67_5322+69del
XM_017018375.2:c.5310+67_5310+69del (SBF2)	XP_016873864.1:n.5310+67_5310+69del
XR_001747994.2:n.5558+67_5558+69del (SBF2)
XR_001748470.1:n.200+866_200+868del
XR_001748471.1:n.85+866_85+868del
NM_001386339.1:c.5547+67_5547+69del (SBF2)	NP_001373268.1:n.5547+67_5547+69del
NM_001386342.1:c.5322+67_5322+69del (SBF2)	NP_001373271.1:n.5322+67_5322+69del
NM_030962.4:c.5451+67_5451+69del (SBF2) MANE Select	NP_112224.1:n.5451+67_5451+69del