Canonical Allele Identifier: CA10316713

Gene: SBF1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50459981C>A , CM000684.2:g.50459981C>A	GRCh38
NC_000022.10:g.50898410C>A , CM000684.1:g.50898410C>A	GRCh37
NC_000022.9:g.49245276C>A	NCBI36
NG_041810.1:g.20091G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.3462G>T	ENSP00000252027.8:p.Pro1154=
ENST00000470434.2:n.59G>T
ENST00000684986.1:c.3465G>T	ENSP00000509117.1:p.Pro1155=
ENST00000685180.1:n.2488+553G>T
ENST00000685386.1:c.1305G>T	ENSP00000510338.1:p.Pro435=
ENST00000685390.1:n.1705G>T
ENST00000685809.1:c.3453G>T	ENSP00000508863.1:p.Pro1151=
ENST00000686191.1:n.159G>T
ENST00000686222.1:c.*2884G>T	ENSP00000508737.1:n.*2884G>T
ENST00000686427.1:c.*475G>T	ENSP00000510379.1:n.*475G>T
ENST00000686801.1:c.3450G>T	ENSP00000509915.1:p.Pro1150=
ENST00000687016.1:c.3441G>T	ENSP00000509074.1:p.Pro1147=
ENST00000687704.1:c.*1276G>T	ENSP00000510454.1:n.*1276G>T
ENST00000687861.1:n.20G>T
ENST00000688066.1:c.3462G>T	ENSP00000510782.1:p.Pro1154=
ENST00000688124.1:c.*2456G>T	ENSP00000510645.1:n.*2456G>T
ENST00000688848.1:c.*2884G>T	ENSP00000509419.1:n.*2884G>T
ENST00000688985.1:c.468G>T	ENSP00000510477.1:p.Pro156=
ENST00000689129.1:c.3465G>T	ENSP00000510414.1:p.Pro1155=
ENST00000689177.1:n.1313G>T
ENST00000689981.1:c.3462G>T	ENSP00000509035.1:p.Pro1154=
ENST00000690369.1:n.3480G>T
ENST00000690590.1:n.224G>T
ENST00000690990.1:c.3456G>T	ENSP00000510461.1:p.Pro1152=
ENST00000691233.1:c.3459G>T	ENSP00000509215.1:p.Pro1153=
ENST00000691345.1:n.1784+291G>T
ENST00000691792.1:c.3462G>T	ENSP00000509911.1:p.Pro1154=
ENST00000691959.1:n.3341G>T
ENST00000692006.1:c.468G>T	ENSP00000509653.1:p.Pro156=
ENST00000692844.1:n.339G>T
ENST00000693052.1:c.3462G>T	ENSP00000509558.1:p.Pro1154=
ENST00000693440.1:c.3459G>T	ENSP00000509462.1:p.Pro1153=
ENST00000693499.1:n.3665G>T
ENST00000380817.8:c.3462G>T MANE Select	ENSP00000370196.2:p.Pro1154=
ENST00000348911.10:c.3465G>T	ENSP00000252027.7:p.Pro1155=
ENST00000380817.7:c.3462G>T	ENSP00000370196.2:p.Pro1154=
NM_002972.3:c.3462G>T	NP_002963.2:p.Pro1154=
XM_005261931.1:c.3465G>T	XP_005261988.1:p.Pro1155=
XM_005261935.1:c.3462G>T	XP_005261992.1:p.Pro1154=
XM_011530707.1:c.3564G>T	XP_011529009.1:p.Pro1188=
XM_011530708.1:c.3516G>T	XP_011529010.1:p.Pro1172=
XM_011530709.1:c.3492G>T	XP_011529011.1:p.Pro1164=
XM_011530710.1:c.3489G>T	XP_011529012.1:p.Pro1163=
XM_011530711.1:c.3567G>T	XP_011529013.1:p.Pro1189=
XR_938344.1:n.3582G>T
NM_001365819.1:c.3465G>T	NP_001352748.1:p.Pro1155=
XM_005261935.2:c.3462G>T	XP_005261992.1:p.Pro1154=
XM_011530709.2:c.3492G>T	XP_011529011.1:p.Pro1164=
XM_011530710.2:c.3489G>T	XP_011529012.1:p.Pro1163=
XM_017028905.2:c.3492G>T	XP_016884394.1:p.Pro1164=
NM_002972.4:c.3462G>T MANE Select	NP_002963.2:p.Pro1154=