Canonical Allele Identifier: CA515383617

Gene: SBF1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50461563C>T , CM000684.2:g.50461563C>T	GRCh38
NC_000022.10:g.50899992C>T , CM000684.1:g.50899992C>T	GRCh37
NC_000022.9:g.49246858C>T	NCBI36
NG_041810.1:g.18509G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.2799G>A	ENSP00000252027.8:p.Thr933=
ENST00000684986.1:c.2802G>A	ENSP00000509117.1:p.Thr934=
ENST00000685180.1:n.2309+384G>A
ENST00000685386.1:c.669G>A	ENSP00000510338.1:p.Thr223=
ENST00000685390.1:n.1042G>A
ENST00000685809.1:c.2790G>A	ENSP00000508863.1:p.Thr930=
ENST00000686222.1:c.*2221G>A	ENSP00000508737.1:n.*2221G>A
ENST00000686427.1:c.2799G>A	ENSP00000510379.1:p.Thr933=
ENST00000686801.1:c.2787G>A	ENSP00000509915.1:p.Thr929=
ENST00000687016.1:c.2778G>A	ENSP00000509074.1:p.Thr926=
ENST00000687704.1:c.*613G>A	ENSP00000510454.1:n.*613G>A
ENST00000688030.1:c.608G>A	ENSP00000508668.1:p.Arg203His
ENST00000688066.1:c.2799G>A	ENSP00000510782.1:p.Thr933=
ENST00000688124.1:c.*1793G>A	ENSP00000510645.1:n.*1793G>A
ENST00000688848.1:c.*2221G>A	ENSP00000509419.1:n.*2221G>A
ENST00000689129.1:c.2802G>A	ENSP00000510414.1:p.Thr934=
ENST00000689177.1:n.650G>A
ENST00000689981.1:c.2799G>A	ENSP00000509035.1:p.Thr933=
ENST00000690369.1:n.2817G>A
ENST00000690990.1:c.2793G>A	ENSP00000510461.1:p.Thr931=
ENST00000691233.1:c.2796G>A	ENSP00000509215.1:p.Thr932=
ENST00000691345.1:n.1300G>A
ENST00000691792.1:c.2799G>A	ENSP00000509911.1:p.Thr933=
ENST00000691959.1:n.2678G>A
ENST00000693052.1:c.2799G>A	ENSP00000509558.1:p.Thr933=
ENST00000693440.1:c.2796G>A	ENSP00000509462.1:p.Thr932=
ENST00000693499.1:n.2444G>A
ENST00000380817.8:c.2799G>A MANE Select	ENSP00000370196.2:p.Thr933=
ENST00000348911.10:c.2802G>A	ENSP00000252027.7:p.Thr934=
ENST00000380817.7:c.2799G>A	ENSP00000370196.2:p.Thr933=
NM_002972.3:c.2799G>A	NP_002963.2:p.Thr933=
XM_005261931.1:c.2802G>A	XP_005261988.1:p.Thr934=
XM_005261935.1:c.2799G>A	XP_005261992.1:p.Thr933=
XM_011530707.1:c.2901G>A	XP_011529009.1:p.Thr967=
XM_011530708.1:c.2853G>A	XP_011529010.1:p.Thr951=
XM_011530709.1:c.2829G>A	XP_011529011.1:p.Thr943=
XM_011530710.1:c.2826G>A	XP_011529012.1:p.Thr942=
XM_011530711.1:c.2904G>A	XP_011529013.1:p.Thr968=
XR_938344.1:n.2919G>A
NM_001365819.1:c.2802G>A	NP_001352748.1:p.Thr934=
XM_005261935.2:c.2799G>A	XP_005261992.1:p.Thr933=
XM_011530709.2:c.2829G>A	XP_011529011.1:p.Thr943=
XM_011530710.2:c.2826G>A	XP_011529012.1:p.Thr942=
XM_017028905.2:c.2829G>A	XP_016884394.1:p.Thr943=
NM_002972.4:c.2799G>A MANE Select	NP_002963.2:p.Thr933=