Canonical Allele Identifier: CA1139768515
Gene: SBF2 HGNC NCBI
SBF2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9785285_9785286del , CM000673.2:g.9785285_9785286del GRCh38
NC_000011.9:g.9806832_9806833del , CM000673.1:g.9806832_9806833del GRCh37
NC_000011.8:g.9763408_9763409del NCBI36
NG_008074.1:g.513925_513926del , LRG_267:g.513925_513926del

Transcript Alleles

HGVS Amino-acid Change
ENST00000524961.6:n.1557_1558del (SBF2)
ENST00000529587.2:n.67_68del (SBF2)
ENST00000532095.2:n.1609_1610del (SBF2)
ENST00000675281.2:c.5148_5149del (SBF2) ENSP00000502491.1:p.Ser1717TyrfsTer?
ENST00000676324.2:c.*1381_*1382del (SBF2) ENSP00000502578.1:n.*1381_*1382del
ENST00000676387.2:c.5130_5131del (SBF2) ENSP00000502779.1:p.Ser1711TyrfsTer?
ENST00000688344.1:c.4680_4681del (SBF2) ENSP00000509987.1:p.Ser1561TyrfsTer?
ENST00000689128.1:c.5169_5170del (SBF2) ENSP00000509587.1:p.Ser1724TyrfsTer?
ENST00000689258.1:c.5010_5011del (SBF2) ENSP00000510475.1:p.Ser1671TyrfsTer?
ENST00000689342.1:c.1239_1240del (SBF2)
ENST00000689356.1:n.2244_2245del (SBF2)
ENST00000689597.1:c.3777_3778del (SBF2) ENSP00000510781.1:p.Ser1260TyrfsTer?
ENST00000689940.1:c.5067_5068del (SBF2) ENSP00000508452.1:p.Ser1690TyrfsTer?
ENST00000690944.1:c.1153_1154del (SBF2)
ENST00000691616.1:n.1549_1550del (SBF2)
ENST00000692716.1:c.4944_4945del (SBF2) ENSP00000509545.1:p.Ser1649TyrfsTer?
ENST00000693541.1:n.1992_1993del (SBF2)
ENST00000256190.13:c.5073_5074del (SBF2) MANE Select ENSP00000256190.8:p.Ser1692TyrfsTer?
ENST00000675281.1:c.5148_5149del (SBF2) ENSP00000502491.1:p.Ser1717TyrfsTer?
ENST00000676324.1:c.*1381_*1382del (SBF2) ENSP00000502578.1:n.*1381_*1382del
ENST00000676387.1:c.5130_5131del (SBF2) ENSP00000502779.1:p.Ser1711TyrfsTer?
ENST00000256190.12:c.5073_5074del (SBF2) ENSP00000256190.8:p.Ser1692TyrfsTer?
ENST00000525040.5:n.376_377del (SBF2)
ENST00000529587.1:n.67_68del (SBF2)
ENST00000532095.1:c.237_238del (SBF2) ENSP00000434620.1:p.Ser80TyrfsTer?
ENST00000617179.4:c.4932_4933del (SBF2) ENSP00000482806.1:p.Ser1645TyrfsTer?
NM_030962.3:c.5073_5074del , LRG_267t1:c.5073_5074del (SBF2) NP_112224.1:p.Ser1692TyrfsTer?
NR_036485.1:n.212-22563_212-22562del (SBF2-AS1)
XM_005253154.3:c.5169_5170del (SBF2) XP_005253211.1:p.Ser1724TyrfsTer?
XM_005253155.3:c.5040_5041del (SBF2) XP_005253212.1:p.Ser1681TyrfsTer?
XM_011520394.1:c.5055_5056del (SBF2) XP_011518696.1:p.Ser1686TyrfsTer?
XR_931024.1:n.455+509_455+510del
XR_931025.1:n.270+2176_270+2177del
XM_005253154.5:c.5169_5170del (SBF2) XP_005253211.1:p.Ser1724TyrfsTer?
XM_005253155.5:c.5040_5041del (SBF2) XP_005253212.1:p.Ser1681TyrfsTer?
XM_011520394.3:c.5055_5056del (SBF2) XP_011518696.1:p.Ser1686TyrfsTer?
XM_017018372.2:c.5031_5032del (SBF2) XP_016873861.1:p.Ser1678TyrfsTer?
XM_017018373.2:c.5031_5032del (SBF2) XP_016873862.1:p.Ser1678TyrfsTer?
XM_017018374.2:c.4944_4945del (SBF2) XP_016873863.1:p.Ser1649TyrfsTer?
XM_017018375.2:c.4932_4933del (SBF2) XP_016873864.1:p.Ser1645TyrfsTer?
XR_001747994.2:n.5180_5181del (SBF2)
NM_001386339.1:c.5169_5170del (SBF2) NP_001373268.1:p.Ser1724TyrfsTer?
NM_001386342.1:c.4944_4945del (SBF2) NP_001373271.1:p.Ser1649TyrfsTer?
NM_030962.4:c.5073_5074del (SBF2) MANE Select NP_112224.1:p.Ser1692TyrfsTer?