Canonical Allele Identifier: CA5881696

Gene: SBF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9895979G>A , CM000673.2:g.9895979G>A	GRCh38
NC_000011.9:g.9917526G>A , CM000673.1:g.9917526G>A	GRCh37
NC_000011.8:g.9874102G>A	NCBI36
NG_008074.1:g.403229C>T , LRG_267:g.403229C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420722.3:c.597C>T	ENSP00000410478.3:p.Ala199=
ENST00000530741.2:c.597C>T	ENSP00000432643.2:p.Ala199=
ENST00000533770.6:c.1893C>T	ENSP00000509247.1:p.Ala631=
ENST00000675281.2:c.1893C>T	ENSP00000502491.1:p.Ala631=
ENST00000676324.2:c.1893C>T	ENSP00000502578.1:p.Ala631=
ENST00000676387.2:c.1779C>T	ENSP00000502779.1:p.Ala593=
ENST00000687210.1:c.*515C>T	ENSP00000509480.1:n.*515C>T
ENST00000688344.1:c.1500C>T	ENSP00000509987.1:p.Ala500=
ENST00000688417.1:n.2043C>T
ENST00000689128.1:c.1893C>T	ENSP00000509587.1:p.Ala631=
ENST00000689258.1:c.1755C>T	ENSP00000510475.1:p.Ala585=
ENST00000689597.1:c.597C>T	ENSP00000510781.1:p.Ala199=
ENST00000689674.1:c.597C>T	ENSP00000510723.1:p.Ala199=
ENST00000689940.1:c.1893C>T	ENSP00000508452.1:p.Ala631=
ENST00000690003.1:c.597C>T	ENSP00000508748.1:p.Ala199=
ENST00000692716.1:c.1764C>T	ENSP00000509545.1:p.Ala588=
ENST00000693181.1:c.597C>T	ENSP00000510179.1:p.Ala199=
ENST00000256190.13:c.1893C>T MANE Select	ENSP00000256190.8:p.Ala631=
ENST00000675281.1:c.1893C>T	ENSP00000502491.1:p.Ala631=
ENST00000676324.1:c.1893C>T	ENSP00000502578.1:p.Ala631=
ENST00000676387.1:c.1779C>T	ENSP00000502779.1:p.Ala593=
ENST00000256190.12:c.1893C>T	ENSP00000256190.8:p.Ala631=
ENST00000420722.2:c.712C>T
ENST00000533770.5:n.1808C>T
ENST00000617179.4:c.1752C>T	ENSP00000482806.1:p.Ala584=
NM_030962.3:c.1893C>T , LRG_267t1:c.1893C>T	NP_112224.1:p.Ala631=
NR_120539.1:n.136-19627G>A
XM_005253154.3:c.1893C>T	XP_005253211.1:p.Ala631=
XM_005253155.3:c.1764C>T	XP_005253212.1:p.Ala588=
XM_011520394.1:c.1779C>T	XP_011518696.1:p.Ala593=
XM_011520395.1:c.1893C>T	XP_011518697.1:p.Ala631=
XM_011520396.1:c.1893C>T	XP_011518698.1:p.Ala631=
XM_005253154.5:c.1893C>T	XP_005253211.1:p.Ala631=
XM_005253155.5:c.1764C>T	XP_005253212.1:p.Ala588=
XM_011520394.3:c.1779C>T	XP_011518696.1:p.Ala593=
XM_011520395.3:c.1893C>T	XP_011518697.1:p.Ala631=
XM_011520396.3:c.1893C>T	XP_011518698.1:p.Ala631=
XM_017018372.2:c.1755C>T	XP_016873861.1:p.Ala585=
XM_017018373.2:c.1755C>T	XP_016873862.1:p.Ala585=
XM_017018374.2:c.1764C>T	XP_016873863.1:p.Ala588=
XM_017018375.2:c.1893C>T	XP_016873864.1:p.Ala631=
XM_017018376.2:c.1893C>T	XP_016873865.1:p.Ala631=
XM_017018377.2:c.1893C>T	XP_016873866.1:p.Ala631=
XR_001747994.2:n.2031C>T
NM_001386339.1:c.1893C>T	NP_001373268.1:p.Ala631=
NM_001386342.1:c.1764C>T	NP_001373271.1:p.Ala588=
NM_030962.4:c.1893C>T MANE Select	NP_112224.1:p.Ala631=