Canonical Allele Identifier: CA1951790096

Gene: SBF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9832209_9832211delinsTAG , CM000673.2:g.9832209_9832211delinsTAG	GRCh38
NC_000011.9:g.9853756_9853758delinsTAG , CM000673.1:g.9853756_9853758delinsTAG	GRCh37
NC_000011.8:g.9810332_9810334delinsTAG	NCBI36
NG_008074.1:g.466997_466999delinsCTA , LRG_267:g.466997_466999delinsCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000530741.2:c.2356+13_2356+15delinsCTA	ENSP00000432643.2:n.2356+13_2356+15delins...
ENST00000675281.2:c.3652+13_3652+15delinsCTA	ENSP00000502491.1:n.3652+13_3652+15delins...
ENST00000676324.2:c.3652+13_3652+15delinsCTA	ENSP00000502578.1:n.3652+13_3652+15delins...
ENST00000676387.2:c.3538+13_3538+15delinsCTA	ENSP00000502779.1:n.3538+13_3538+15delins...
ENST00000688344.1:c.3259+13_3259+15delinsCTA	ENSP00000509987.1:n.3259+13_3259+15delins...
ENST00000689128.1:c.3652+13_3652+15delinsCTA	ENSP00000509587.1:n.3652+13_3652+15delins...
ENST00000689258.1:c.3514+13_3514+15delinsCTA	ENSP00000510475.1:n.3514+13_3514+15delins...
ENST00000689356.1:n.823+13_823+15delinsCTA
ENST00000689597.1:c.2356+13_2356+15delinsCTA	ENSP00000510781.1:n.2356+13_2356+15delins...
ENST00000689940.1:c.3646+13_3646+15delinsCTA	ENSP00000508452.1:n.3646+13_3646+15delins...
ENST00000692716.1:c.3523+13_3523+15delinsCTA	ENSP00000509545.1:n.3523+13_3523+15delins...
ENST00000256190.13:c.3652+13_3652+15delinsCTA MANE Select	ENSP00000256190.8:n.3652+13_3652+15delins...
ENST00000675281.1:c.3652+13_3652+15delinsCTA	ENSP00000502491.1:n.3652+13_3652+15delins...
ENST00000676324.1:c.3652+13_3652+15delinsCTA	ENSP00000502578.1:n.3652+13_3652+15delins...
ENST00000676387.1:c.3538+13_3538+15delinsCTA	ENSP00000502779.1:n.3538+13_3538+15delins...
ENST00000256190.12:c.3652+13_3652+15delinsCTA	ENSP00000256190.8:n.3652+13_3652+15delins...
ENST00000530741.1:c.303+13_303+15delinsCTA
ENST00000617179.4:c.3511+13_3511+15delinsCTA	ENSP00000482806.1:n.3511+13_3511+15delins...
NM_030962.3:c.3652+13_3652+15delinsCTA , LRG_267t1:c.3652+13_3652+15delinsCTA	NP_112224.1:n.3652+13_3652+15delinsCTA
XM_005253154.3:c.3652+13_3652+15delinsCTA	XP_005253211.1:n.3652+13_3652+15delinsCTA...
XM_005253155.3:c.3523+13_3523+15delinsCTA	XP_005253212.1:n.3523+13_3523+15delinsCTA...
XM_011520394.1:c.3538+13_3538+15delinsCTA	XP_011518696.1:n.3538+13_3538+15delinsCTA...
XM_011520395.1:c.3652+13_3652+15delinsCTA	XP_011518697.1:n.3652+13_3652+15delinsCTA...
XM_005253154.5:c.3652+13_3652+15delinsCTA	XP_005253211.1:n.3652+13_3652+15delinsCTA...
XM_005253155.5:c.3523+13_3523+15delinsCTA	XP_005253212.1:n.3523+13_3523+15delinsCTA...
XM_011520394.3:c.3538+13_3538+15delinsCTA	XP_011518696.1:n.3538+13_3538+15delinsCTA...
XM_011520395.3:c.3652+13_3652+15delinsCTA	XP_011518697.1:n.3652+13_3652+15delinsCTA...
XM_017018372.2:c.3514+13_3514+15delinsCTA	XP_016873861.1:n.3514+13_3514+15delinsCTA...
XM_017018373.2:c.3514+13_3514+15delinsCTA	XP_016873862.1:n.3514+13_3514+15delinsCTA...
XM_017018374.2:c.3523+13_3523+15delinsCTA	XP_016873863.1:n.3523+13_3523+15delinsCTA...
XM_017018375.2:c.3652+13_3652+15delinsCTA	XP_016873864.1:n.3652+13_3652+15delinsCTA...
XM_017018376.2:c.3652+13_3652+15delinsCTA	XP_016873865.1:n.3652+13_3652+15delinsCTA...
XR_001747994.2:n.3790+13_3790+15delinsCTA
NM_001386339.1:c.3652+13_3652+15delinsCTA	NP_001373268.1:n.3652+13_3652+15delinsCTA...
NM_001386342.1:c.3523+13_3523+15delinsCTA	NP_001373271.1:n.3523+13_3523+15delinsCTA...
NM_030962.4:c.3652+13_3652+15delinsCTA MANE Select	NP_112224.1:n.3652+13_3652+15delinsCTA