Canonical Allele Identifier: CA10316502

Gene: SBF1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50457029G>C , CM000684.2:g.50457029G>C	GRCh38
NC_000022.10:g.50895458G>C , CM000684.1:g.50895458G>C	GRCh37
NC_000022.9:g.49242324G>C	NCBI36
NG_041810.1:g.23043C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.3827-356C>G	ENSP00000252027.8:n.3827-356C>G
ENST00000470434.2:n.227-356C>G
ENST00000684986.1:c.3907+5C>G	ENSP00000509117.1:n.3907+5C>G
ENST00000685180.1:n.2488+3505C>G
ENST00000685390.1:n.1873-356C>G
ENST00000685592.1:c.139-356C>G
ENST00000685809.1:c.3818-356C>G	ENSP00000508863.1:n.3818-356C>G
ENST00000686191.1:n.2749C>G
ENST00000686222.1:c.*3326+5C>G	ENSP00000508737.1:n.*3326+5C>G
ENST00000686427.1:c.*840-356C>G	ENSP00000510379.1:n.*840-356C>G
ENST00000686758.1:n.1211C>G
ENST00000686801.1:c.3892+5C>G	ENSP00000509915.1:n.3892+5C>G
ENST00000686826.1:n.221+5C>G
ENST00000687016.1:c.3806-356C>G	ENSP00000509074.1:n.3806-356C>G
ENST00000687704.1:c.*1630-356C>G	ENSP00000510454.1:n.*1630-356C>G
ENST00000687861.1:n.467C>G
ENST00000688066.1:c.3904+5C>G	ENSP00000510782.1:n.3904+5C>G
ENST00000688124.1:c.*2821-356C>G	ENSP00000510645.1:n.*2821-356C>G
ENST00000688848.1:c.*3249-356C>G	ENSP00000509419.1:n.*3249-356C>G
ENST00000688985.1:c.910+5C>G	ENSP00000510477.1:n.910+5C>G
ENST00000689129.1:c.3830-356C>G	ENSP00000510414.1:n.3830-356C>G
ENST00000689177.1:n.4188C>G
ENST00000689981.1:c.3904+5C>G	ENSP00000509035.1:n.3904+5C>G
ENST00000690369.1:n.3922+5C>G
ENST00000690590.1:n.951+5C>G
ENST00000690990.1:c.3898+5C>G	ENSP00000510461.1:n.3898+5C>G
ENST00000691233.1:c.3824-356C>G	ENSP00000509215.1:n.3824-356C>G
ENST00000691345.1:n.1941-356C>G
ENST00000691792.1:c.3904+5C>G	ENSP00000509911.1:n.3904+5C>G
ENST00000691959.1:n.3991-356C>G
ENST00000692844.1:n.989-356C>G
ENST00000693052.1:c.3922+5C>G	ENSP00000509558.1:n.3922+5C>G
ENST00000693289.1:n.708C>G
ENST00000693440.1:c.3901+5C>G	ENSP00000509462.1:n.3901+5C>G
ENST00000693499.1:n.4474C>G
ENST00000693591.1:n.1653C>G
ENST00000380817.8:c.3904+5C>G MANE Select	ENSP00000370196.2:n.3904+5C>G
ENST00000348911.10:c.3830-356C>G	ENSP00000252027.7:n.3830-356C>G
ENST00000380817.7:c.3904+5C>G	ENSP00000370196.2:n.3904+5C>G
ENST00000476293.1:n.314+5C>G
NM_002972.3:c.3904+5C>G	NP_002963.2:n.3904+5C>G
XM_005261931.1:c.3907+5C>G	XP_005261988.1:n.3907+5C>G
XM_005261935.1:c.3827-356C>G	XP_005261992.1:n.3827-356C>G
XM_011530707.1:c.4006+5C>G	XP_011529009.1:n.4006+5C>G
XM_011530708.1:c.3958+5C>G	XP_011529010.1:n.3958+5C>G
XM_011530709.1:c.3934+5C>G	XP_011529011.1:n.3934+5C>G
XM_011530710.1:c.3931+5C>G	XP_011529012.1:n.3931+5C>G
XM_011530711.1:c.3932-356C>G	XP_011529013.1:n.3932-356C>G
XR_938344.1:n.4024+5C>G
NM_001365819.1:c.3830-356C>G	NP_001352748.1:n.3830-356C>G
XM_005261935.2:c.3827-356C>G	XP_005261992.1:n.3827-356C>G
XM_011530709.2:c.3934+5C>G	XP_011529011.1:n.3934+5C>G
XM_011530710.2:c.3931+5C>G	XP_011529012.1:n.3931+5C>G
XM_017028905.2:c.3857-356C>G	XP_016884394.1:n.3857-356C>G
NM_002972.4:c.3904+5C>G MANE Select	NP_002963.2:n.3904+5C>G