Canonical Allele Identifier: CA412194618

Gene: SBF1

Linked Data

• MyVariant Identifiers: chr22:g.50893522T>A (hg19) ; chr22:g.50455093T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455093T>A , CM000684.2:g.50455093T>A	GRCh38
NC_000022.10:g.50893522T>A , CM000684.1:g.50893522T>A	GRCh37
NC_000022.9:g.49240388T>A	NCBI36
NG_041810.1:g.24979A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4526A>T	ENSP00000252027.8:p.Lys1509Met
ENST00000418590.4:c.236A>T	ENSP00000401538.2:p.Lys79Met
ENST00000470434.2:n.1007A>T
ENST00000684986.1:c.4607A>T	ENSP00000509117.1:p.Lys1536Met
ENST00000685180.1:n.2488+5441A>T
ENST00000685390.1:n.2572A>T
ENST00000685411.1:n.354A>T
ENST00000685592.1:c.838A>T
ENST00000685809.1:c.4517A>T	ENSP00000508863.1:p.Lys1506Met
ENST00000686029.1:c.682A>T
ENST00000686191.1:n.3804A>T
ENST00000686222.1:c.*4026A>T	ENSP00000508737.1:n.*4026A>T
ENST00000686321.1:c.700A>T
ENST00000686427.1:c.*1539A>T	ENSP00000510379.1:n.*1539A>T
ENST00000686758.1:n.2347A>T
ENST00000686801.1:c.4592A>T	ENSP00000509915.1:p.Lys1531Met
ENST00000686826.1:n.923A>T
ENST00000687016.1:c.4505A>T	ENSP00000509074.1:p.Lys1502Met
ENST00000687704.1:c.*2329A>T	ENSP00000510454.1:n.*2329A>T
ENST00000688066.1:c.4604A>T	ENSP00000510782.1:p.Lys1535Met
ENST00000688124.1:c.*3522A>T	ENSP00000510645.1:n.*3522A>T
ENST00000688848.1:c.*3948A>T	ENSP00000509419.1:n.*3948A>T
ENST00000688985.1:c.1605A>T	ENSP00000510477.1:n.1605A>T
ENST00000689129.1:c.4529A>T	ENSP00000510414.1:p.Lys1510Met
ENST00000689177.1:n.5876A>T
ENST00000689849.1:c.700A>T
ENST00000689981.1:c.4604A>T	ENSP00000509035.1:p.Lys1535Met
ENST00000690369.1:n.4622A>T
ENST00000690590.1:n.1651A>T
ENST00000690990.1:c.4598A>T	ENSP00000510461.1:p.Lys1533Met
ENST00000691233.1:c.4523A>T	ENSP00000509215.1:p.Lys1508Met
ENST00000691306.1:c.702A>T
ENST00000691345.1:n.2302+1123A>T
ENST00000691792.1:c.4592A>T	ENSP00000509911.1:p.Lys1531Met
ENST00000691959.1:n.5323A>T
ENST00000692844.1:n.1688A>T
ENST00000692946.1:c.700A>T
ENST00000693052.1:c.4622A>T	ENSP00000509558.1:p.Lys1541Met
ENST00000693289.1:n.1763A>T
ENST00000693440.1:c.4601A>T	ENSP00000509462.1:p.Lys1534Met
ENST00000693499.1:n.5529A>T
ENST00000693591.1:n.3341A>T
ENST00000380817.8:c.4604A>T MANE Select	ENSP00000370196.2:p.Lys1535Met
ENST00000348911.10:c.4529A>T	ENSP00000252027.7:p.Lys1510Met
ENST00000380817.7:c.4604A>T	ENSP00000370196.2:p.Lys1535Met
ENST00000418590.3:c.204A>T
ENST00000470434.1:n.745A>T
NM_002972.3:c.4604A>T	NP_002963.2:p.Lys1535Met
XM_005261931.1:c.4607A>T	XP_005261988.1:p.Lys1536Met
XM_005261935.1:c.4526A>T	XP_005261992.1:p.Lys1509Met
XM_011530707.1:c.4706A>T	XP_011529009.1:p.Lys1569Met
XM_011530708.1:c.4658A>T	XP_011529010.1:p.Lys1553Met
XM_011530709.1:c.4634A>T	XP_011529011.1:p.Lys1545Met
XM_011530710.1:c.4631A>T	XP_011529012.1:p.Lys1544Met
XM_011530711.1:c.4631A>T	XP_011529013.1:p.Lys1544Met
XR_938344.1:n.4724A>T
NM_001365819.1:c.4529A>T	NP_001352748.1:p.Lys1510Met
XM_005261935.2:c.4526A>T	XP_005261992.1:p.Lys1509Met
XM_011530709.2:c.4634A>T	XP_011529011.1:p.Lys1545Met
XM_011530710.2:c.4631A>T	XP_011529012.1:p.Lys1544Met
XM_017028905.2:c.4556A>T	XP_016884394.1:p.Lys1519Met
NM_002972.4:c.4604A>T MANE Select	NP_002963.2:p.Lys1535Met