Canonical Allele Identifier: CA1951783206

Gene: SBF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9816961A= , CM000673.2:g.9816961A=	GRCh38
NC_000011.9:g.9838508A= , CM000673.1:g.9838508A=	GRCh37
NC_000011.8:g.9795084A=	NCBI36
NG_008074.1:g.482247T= , LRG_267:g.482247T=

Transcript Alleles

HGVS	Amino-acid Change
NM_030962.4:c.3857T= MANE Select	NP_112224.1:p.Val1286=
ENST00000256190.13:c.3857T= MANE Select	ENSP00000256190.8:p.Val1286=
NM_001386339.1:c.3953T=	NP_001373268.1:p.Val1318=
NM_001386342.1:c.3728T=	NP_001373271.1:p.Val1243=
NM_030962.3:c.3857T= , LRG_267t1:c.3857T=	NP_112224.1:p.Val1286=
ENST00000256190.12:c.3857T=	ENSP00000256190.8:p.Val1286=
ENST00000524961.5:n.341T=
ENST00000524961.6:n.341T=
ENST00000530741.1:c.604T=
ENST00000530741.2:c.2420T=	ENSP00000432643.2:p.Val807=
ENST00000532095.2:n.393T=
ENST00000533584.1:n.377T=
ENST00000617179.4:c.3716T=	ENSP00000482806.1:p.Val1239=
ENST00000675281.1:c.3932T=	ENSP00000502491.1:p.Val1311=
ENST00000675281.2:c.3932T=	ENSP00000502491.1:p.Val1311=
ENST00000676324.1:c.*165T=	ENSP00000502578.1:n.*165T=
ENST00000676324.2:c.*165T=	ENSP00000502578.1:n.*165T=
ENST00000676387.1:c.3914T=	ENSP00000502779.1:p.Val1305=
ENST00000676387.2:c.3914T=	ENSP00000502779.1:p.Val1305=
ENST00000688344.1:c.3464T=	ENSP00000509987.1:p.Val1155=
ENST00000689128.1:c.3953T=	ENSP00000509587.1:p.Val1318=
ENST00000689258.1:c.3794T=	ENSP00000510475.1:p.Val1265=
ENST00000689342.1:c.64T=
ENST00000689356.1:n.1028T=
ENST00000689597.1:c.2561T=	ENSP00000510781.1:p.Val854=
ENST00000689940.1:c.3851T=	ENSP00000508452.1:p.Val1284=
ENST00000690944.1:c.64T=
ENST00000691616.1:n.341T=
ENST00000692716.1:c.3728T=	ENSP00000509545.1:p.Val1243=
ENST00000693541.1:n.776T=
XM_005253154.3:c.3953T=	XP_005253211.1:p.Val1318=
XM_005253154.5:c.3953T=	XP_005253211.1:p.Val1318=
XM_005253155.3:c.3824T=	XP_005253212.1:p.Val1275=
XM_005253155.5:c.3824T=	XP_005253212.1:p.Val1275=
XM_011520394.1:c.3839T=	XP_011518696.1:p.Val1280=
XM_011520394.3:c.3839T=	XP_011518696.1:p.Val1280=
XM_017018372.2:c.3815T=	XP_016873861.1:p.Val1272=
XM_017018373.2:c.3815T=	XP_016873862.1:p.Val1272=
XM_017018374.2:c.3728T=	XP_016873863.1:p.Val1243=
XM_017018375.2:c.3716T=	XP_016873864.1:p.Val1239=
XR_001747994.2:n.4091T=