Canonical Allele Identifier: CA379632617

Gene: SBF2 SBF2-AS1

Linked Data

• MyVariant Identifiers: chr11:g.9787656_9787658del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9787656_9787658del , CM000673.2:g.9787656_9787658del	GRCh38
NC_000011.9:g.9809203_9809205del , CM000673.1:g.9809203_9809205del	GRCh37
NC_000011.8:g.9765779_9765781del	NCBI36
NG_008074.1:g.511550_511552del , LRG_267:g.511550_511552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1497_1499del (SBF2)
ENST00000532095.2:n.1549_1551del (SBF2)
ENST00000675281.2:c.5088_5090del (SBF2)	ENSP00000502491.1:p.Lys1697del
ENST00000676324.2:c.*1321_*1323del (SBF2)	ENSP00000502578.1:n.*1321_*1323del
ENST00000676387.2:c.5070_5072del (SBF2)	ENSP00000502779.1:p.Lys1691del
ENST00000688344.1:c.4620_4622del (SBF2)	ENSP00000509987.1:p.Lys1541del
ENST00000689128.1:c.5109_5111del (SBF2)	ENSP00000509587.1:p.Lys1704del
ENST00000689258.1:c.4950_4952del (SBF2)	ENSP00000510475.1:p.Lys1651del
ENST00000689342.1:c.1179_1181del (SBF2)
ENST00000689356.1:n.2184_2186del (SBF2)
ENST00000689597.1:c.3717_3719del (SBF2)	ENSP00000510781.1:p.Lys1240del
ENST00000689940.1:c.5007_5009del (SBF2)	ENSP00000508452.1:p.Lys1670del
ENST00000690944.1:c.1093_1095del (SBF2)
ENST00000691616.1:n.1489_1491del (SBF2)
ENST00000692716.1:c.4884_4886del (SBF2)	ENSP00000509545.1:p.Lys1629del
ENST00000693541.1:n.1932_1934del (SBF2)
ENST00000256190.13:c.5013_5015del (SBF2) MANE Select	ENSP00000256190.8:p.Lys1672del
ENST00000675281.1:c.5088_5090del (SBF2)	ENSP00000502491.1:p.Lys1697del
ENST00000676324.1:c.*1321_*1323del (SBF2)	ENSP00000502578.1:n.*1321_*1323del
ENST00000676387.1:c.5070_5072del (SBF2)	ENSP00000502779.1:p.Lys1691del
ENST00000256190.12:c.5013_5015del (SBF2)	ENSP00000256190.8:p.Lys1672del
ENST00000525040.5:n.316_318del (SBF2)
ENST00000532095.1:c.177_179del (SBF2)	ENSP00000434620.1:p.Lys60del
ENST00000617179.4:c.4872_4874del (SBF2)	ENSP00000482806.1:p.Lys1625del
NM_030962.3:c.5013_5015del , LRG_267t1:c.5013_5015del (SBF2)	NP_112224.1:p.Lys1672del
NR_036485.1:n.212-20192_212-20190del (SBF2-AS1)
XM_005253154.3:c.5109_5111del (SBF2)	XP_005253211.1:p.Lys1704del
XM_005253155.3:c.4980_4982del (SBF2)	XP_005253212.1:p.Lys1661del
XM_011520394.1:c.4995_4997del (SBF2)	XP_011518696.1:p.Lys1666del
XR_931024.1:n.455+2880_455+2882del
XR_931025.1:n.271-3213_271-3211del
XM_005253154.5:c.5109_5111del (SBF2)	XP_005253211.1:p.Lys1704del
XM_005253155.5:c.4980_4982del (SBF2)	XP_005253212.1:p.Lys1661del
XM_011520394.3:c.4995_4997del (SBF2)	XP_011518696.1:p.Lys1666del
XM_017018372.2:c.4971_4973del (SBF2)	XP_016873861.1:p.Lys1658del
XM_017018373.2:c.4971_4973del (SBF2)	XP_016873862.1:p.Lys1658del
XM_017018374.2:c.4884_4886del (SBF2)	XP_016873863.1:p.Lys1629del
XM_017018375.2:c.4872_4874del (SBF2)	XP_016873864.1:p.Lys1625del
XR_001747994.2:n.5120_5122del (SBF2)
NM_001386339.1:c.5109_5111del (SBF2)	NP_001373268.1:p.Lys1704del
NM_001386342.1:c.4884_4886del (SBF2)	NP_001373271.1:p.Lys1629del
NM_030962.4:c.5013_5015del (SBF2) MANE Select	NP_112224.1:p.Lys1672del