Canonical Allele Identifier: CA412194541

Gene: SBF1

Linked Data

• MyVariant Identifiers: chr22:g.50893511A>C (hg19) ; chr22:g.50455082A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455082A>C , CM000684.2:g.50455082A>C	GRCh38
NC_000022.10:g.50893511A>C , CM000684.1:g.50893511A>C	GRCh37
NC_000022.9:g.49240377A>C	NCBI36
NG_041810.1:g.24990T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4537T>G	ENSP00000252027.8:p.Tyr1513Asp
ENST00000418590.4:c.247T>G	ENSP00000401538.2:p.Tyr83Asp
ENST00000470434.2:n.1018T>G
ENST00000684986.1:c.4618T>G	ENSP00000509117.1:p.Tyr1540Asp
ENST00000685180.1:n.2488+5452T>G
ENST00000685390.1:n.2583T>G
ENST00000685411.1:n.365T>G
ENST00000685592.1:c.849T>G
ENST00000685809.1:c.4528T>G	ENSP00000508863.1:p.Tyr1510Asp
ENST00000686029.1:c.693T>G
ENST00000686191.1:n.3815T>G
ENST00000686222.1:c.*4037T>G	ENSP00000508737.1:n.*4037T>G
ENST00000686321.1:c.711T>G
ENST00000686427.1:c.*1550T>G	ENSP00000510379.1:n.*1550T>G
ENST00000686758.1:n.2358T>G
ENST00000686801.1:c.4603T>G	ENSP00000509915.1:p.Tyr1535Asp
ENST00000686826.1:n.934T>G
ENST00000687016.1:c.4516T>G	ENSP00000509074.1:p.Tyr1506Asp
ENST00000687704.1:c.*2340T>G	ENSP00000510454.1:n.*2340T>G
ENST00000688066.1:c.4615T>G	ENSP00000510782.1:p.Tyr1539Asp
ENST00000688124.1:c.*3533T>G	ENSP00000510645.1:n.*3533T>G
ENST00000688848.1:c.*3959T>G	ENSP00000509419.1:n.*3959T>G
ENST00000688985.1:c.1616T>G	ENSP00000510477.1:n.1616T>G
ENST00000689129.1:c.4540T>G	ENSP00000510414.1:p.Tyr1514Asp
ENST00000689177.1:n.5887T>G
ENST00000689849.1:c.711T>G
ENST00000689981.1:c.4615T>G	ENSP00000509035.1:p.Tyr1539Asp
ENST00000690369.1:n.4633T>G
ENST00000690590.1:n.1662T>G
ENST00000690990.1:c.4609T>G	ENSP00000510461.1:p.Tyr1537Asp
ENST00000691233.1:c.4534T>G	ENSP00000509215.1:p.Tyr1512Asp
ENST00000691306.1:c.713T>G
ENST00000691345.1:n.2302+1134T>G
ENST00000691792.1:c.4603T>G	ENSP00000509911.1:p.Tyr1535Asp
ENST00000691959.1:n.5334T>G
ENST00000692844.1:n.1699T>G
ENST00000692946.1:c.711T>G
ENST00000693052.1:c.4633T>G	ENSP00000509558.1:p.Tyr1545Asp
ENST00000693289.1:n.1774T>G
ENST00000693440.1:c.4612T>G	ENSP00000509462.1:p.Tyr1538Asp
ENST00000693499.1:n.5540T>G
ENST00000693591.1:n.3352T>G
ENST00000380817.8:c.4615T>G MANE Select	ENSP00000370196.2:p.Tyr1539Asp
ENST00000348911.10:c.4540T>G	ENSP00000252027.7:p.Tyr1514Asp
ENST00000380817.7:c.4615T>G	ENSP00000370196.2:p.Tyr1539Asp
ENST00000418590.3:c.215T>G
ENST00000470434.1:n.756T>G
NM_002972.3:c.4615T>G	NP_002963.2:p.Tyr1539Asp
XM_005261931.1:c.4618T>G	XP_005261988.1:p.Tyr1540Asp
XM_005261935.1:c.4537T>G	XP_005261992.1:p.Tyr1513Asp
XM_011530707.1:c.4717T>G	XP_011529009.1:p.Tyr1573Asp
XM_011530708.1:c.4669T>G	XP_011529010.1:p.Tyr1557Asp
XM_011530709.1:c.4645T>G	XP_011529011.1:p.Tyr1549Asp
XM_011530710.1:c.4642T>G	XP_011529012.1:p.Tyr1548Asp
XM_011530711.1:c.4642T>G	XP_011529013.1:p.Tyr1548Asp
XR_938344.1:n.4735T>G
NM_001365819.1:c.4540T>G	NP_001352748.1:p.Tyr1514Asp
XM_005261935.2:c.4537T>G	XP_005261992.1:p.Tyr1513Asp
XM_011530709.2:c.4645T>G	XP_011529011.1:p.Tyr1549Asp
XM_011530710.2:c.4642T>G	XP_011529012.1:p.Tyr1548Asp
XM_017028905.2:c.4567T>G	XP_016884394.1:p.Tyr1523Asp
NM_002972.4:c.4615T>G MANE Select	NP_002963.2:p.Tyr1539Asp