Canonical Allele Identifier: CA1951768802
Gene: SBF2 HGNC NCBI
SBF2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9781396_9781397delinsCT , CM000673.2:g.9781396_9781397delinsCT GRCh38
NC_000011.9:g.9802943_9802944delinsCT , CM000673.1:g.9802943_9802944delinsCT GRCh37
NC_000011.8:g.9759519_9759520delinsCT NCBI36
NG_008074.1:g.517811_517812delinsAG , LRG_267:g.517811_517812delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000524961.6:n.1935+110_1935+111delinsAG (SBF2)
ENST00000675281.2:c.5526+110_5526+111delinsAG (SBF2) ENSP00000502491.1:n.5526+110_5526+111delinsAG
ENST00000676324.2:c.*1759+110_*1759+111delinsAG (SBF2) ENSP00000502578.1:n.*1759+110_*1759+111delinsAG
ENST00000676387.2:c.5508+110_5508+111delinsAG (SBF2) ENSP00000502779.1:n.5508+110_5508+111delinsAG
ENST00000688344.1:c.5058+110_5058+111delinsAG (SBF2) ENSP00000509987.1:n.5058+110_5058+111delinsAG
ENST00000689128.1:c.5547+110_5547+111delinsAG (SBF2) ENSP00000509587.1:n.5547+110_5547+111delinsAG
ENST00000689258.1:c.5388+110_5388+111delinsAG (SBF2) ENSP00000510475.1:n.5388+110_5388+111delinsAG
ENST00000689342.1:c.1617+110_1617+111delinsAG (SBF2)
ENST00000689356.1:n.2622+110_2622+111delinsAG (SBF2)
ENST00000689940.1:c.5445+110_5445+111delinsAG (SBF2) ENSP00000508452.1:n.5445+110_5445+111delinsAG
ENST00000690437.1:n.1400+110_1400+111delinsAG (SBF2)
ENST00000690944.1:c.1531+110_1531+111delinsAG (SBF2)
ENST00000691616.1:n.1927+110_1927+111delinsAG (SBF2)
ENST00000692716.1:c.5322+110_5322+111delinsAG (SBF2) ENSP00000509545.1:n.5322+110_5322+111delinsAG
ENST00000693541.1:n.2370+110_2370+111delinsAG (SBF2)
ENST00000256190.13:c.5451+110_5451+111delinsAG (SBF2) MANE Select ENSP00000256190.8:n.5451+110_5451+111delinsAG
ENST00000675281.1:c.5526+110_5526+111delinsAG (SBF2) ENSP00000502491.1:n.5526+110_5526+111delinsAG
ENST00000676324.1:c.*1759+110_*1759+111delinsAG (SBF2) ENSP00000502578.1:n.*1759+110_*1759+111delinsAG
ENST00000676387.1:c.5508+110_5508+111delinsAG (SBF2) ENSP00000502779.1:n.5508+110_5508+111delinsAG
ENST00000256190.12:c.5451+110_5451+111delinsAG (SBF2) ENSP00000256190.8:n.5451+110_5451+111delinsAG
ENST00000525040.5:n.754+110_754+111delinsAG (SBF2)
ENST00000617179.4:c.5310+110_5310+111delinsAG (SBF2) ENSP00000482806.1:n.5310+110_5310+111delinsAG
NM_030962.3:c.5451+110_5451+111delinsAG , LRG_267t1:c.5451+110_5451+111delinsAG (SBF2) NP_112224.1:n.5451+110_5451+111delinsAG
NR_036485.1:n.211+22893_211+22894delinsCT (SBF2-AS1)
XM_005253154.3:c.5547+110_5547+111delinsAG (SBF2) XP_005253211.1:n.5547+110_5547+111delinsAG
XM_005253155.3:c.5418+110_5418+111delinsAG (SBF2) XP_005253212.1:n.5418+110_5418+111delinsAG
XM_011520394.1:c.5433+110_5433+111delinsAG (SBF2) XP_011518696.1:n.5433+110_5433+111delinsAG
XR_931024.1:n.200+821_200+822delinsCT
XR_931025.1:n.200+821_200+822delinsCT
XM_005253154.5:c.5547+110_5547+111delinsAG (SBF2) XP_005253211.1:n.5547+110_5547+111delinsAG
XM_005253155.5:c.5418+110_5418+111delinsAG (SBF2) XP_005253212.1:n.5418+110_5418+111delinsAG
XM_011520394.3:c.5433+110_5433+111delinsAG (SBF2) XP_011518696.1:n.5433+110_5433+111delinsAG
XM_017018372.2:c.5409+110_5409+111delinsAG (SBF2) XP_016873861.1:n.5409+110_5409+111delinsAG
XM_017018373.2:c.5409+110_5409+111delinsAG (SBF2) XP_016873862.1:n.5409+110_5409+111delinsAG
XM_017018374.2:c.5322+110_5322+111delinsAG (SBF2) XP_016873863.1:n.5322+110_5322+111delinsAG
XM_017018375.2:c.5310+110_5310+111delinsAG (SBF2) XP_016873864.1:n.5310+110_5310+111delinsAG
XR_001747994.2:n.5558+110_5558+111delinsAG (SBF2)
XR_001748470.1:n.200+821_200+822delinsCT
XR_001748471.1:n.85+821_85+822delinsCT
NM_001386339.1:c.5547+110_5547+111delinsAG (SBF2) NP_001373268.1:n.5547+110_5547+111delinsAG
NM_001386342.1:c.5322+110_5322+111delinsAG (SBF2) NP_001373271.1:n.5322+110_5322+111delinsAG
NM_030962.4:c.5451+110_5451+111delinsAG (SBF2) MANE Select NP_112224.1:n.5451+110_5451+111delinsAG