Canonical Allele Identifier: CA10318273

Gene: SBF1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50474786C>G , CM000684.2:g.50474786C>G	GRCh38
NC_000022.10:g.50913215C>G , CM000684.1:g.50913215C>G	GRCh37
NC_000022.9:g.49260081C>G	NCBI36
NG_041810.1:g.5286G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.55G>C	ENSP00000252027.8:p.Gly19Arg
ENST00000399627.4:n.64G>C
ENST00000684986.1:c.55G>C	ENSP00000509117.1:p.Gly19Arg
ENST00000685180.1:n.132-7093G>C
ENST00000685809.1:c.55G>C	ENSP00000508863.1:p.Gly19Arg
ENST00000686222.1:c.55G>C	ENSP00000508737.1:p.Gly19Arg
ENST00000686427.1:c.55G>C	ENSP00000510379.1:p.Gly19Arg
ENST00000686801.1:c.55G>C	ENSP00000509915.1:p.Gly19Arg
ENST00000687016.1:c.55G>C	ENSP00000509074.1:p.Gly19Arg
ENST00000687704.1:c.55G>C	ENSP00000510454.1:p.Gly19Arg
ENST00000688066.1:c.55G>C	ENSP00000510782.1:p.Gly19Arg
ENST00000688124.1:c.55G>C	ENSP00000510645.1:p.Gly19Arg
ENST00000688848.1:c.55G>C	ENSP00000509419.1:p.Gly19Arg
ENST00000689129.1:c.55G>C	ENSP00000510414.1:p.Gly19Arg
ENST00000689981.1:c.55G>C	ENSP00000509035.1:p.Gly19Arg
ENST00000690155.1:n.241G>C
ENST00000690369.1:n.1G>C
ENST00000690990.1:c.55G>C	ENSP00000510461.1:p.Gly19Arg
ENST00000691233.1:c.55G>C	ENSP00000509215.1:p.Gly19Arg
ENST00000691344.1:c.55G>C	ENSP00000509009.1:p.Gly19Arg
ENST00000691792.1:c.55G>C	ENSP00000509911.1:p.Gly19Arg
ENST00000693052.1:c.55G>C	ENSP00000509558.1:p.Gly19Arg
ENST00000693440.1:c.55G>C	ENSP00000509462.1:p.Gly19Arg
ENST00000380817.8:c.55G>C MANE Select	ENSP00000370196.2:p.Gly19Arg
ENST00000348911.10:c.55G>C	ENSP00000252027.7:p.Gly19Arg
ENST00000380817.7:c.55G>C	ENSP00000370196.2:p.Gly19Arg
ENST00000399627.3:n.64G>C
NM_002972.3:c.55G>C	NP_002963.2:p.Gly19Arg
XM_005261931.1:c.55G>C	XP_005261988.1:p.Gly19Arg
XM_005261935.1:c.55G>C	XP_005261992.1:p.Gly19Arg
XM_011530708.1:c.106+5214G>C	XP_011529010.1:n.106+5214G>C
NM_001365819.1:c.55G>C	NP_001352748.1:p.Gly19Arg
XM_005261935.2:c.55G>C	XP_005261992.1:p.Gly19Arg
NM_002972.4:c.55G>C MANE Select	NP_002963.2:p.Gly19Arg