Canonical Allele Identifier: CA412194066

Gene: SBF1

Linked Data

• MyVariant Identifiers: chr22:g.50893463A>T (hg19) ; chr22:g.50455034A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455034A>T , CM000684.2:g.50455034A>T	GRCh38
NC_000022.10:g.50893463A>T , CM000684.1:g.50893463A>T	GRCh37
NC_000022.9:g.49240329A>T	NCBI36
NG_041810.1:g.25038T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4585T>A	ENSP00000252027.8:p.Tyr1529Asn
ENST00000418590.4:c.295T>A	ENSP00000401538.2:p.Tyr99Asn
ENST00000470434.2:n.1066T>A
ENST00000684986.1:c.4666T>A	ENSP00000509117.1:p.Tyr1556Asn
ENST00000685180.1:n.2488+5500T>A
ENST00000685390.1:n.2631T>A
ENST00000685411.1:n.413T>A
ENST00000685592.1:c.897T>A
ENST00000685809.1:c.4576T>A	ENSP00000508863.1:p.Tyr1526Asn
ENST00000686029.1:c.741T>A
ENST00000686191.1:n.3863T>A
ENST00000686222.1:c.*4085T>A	ENSP00000508737.1:n.*4085T>A
ENST00000686321.1:c.759T>A
ENST00000686427.1:c.*1598T>A	ENSP00000510379.1:n.*1598T>A
ENST00000686758.1:n.2406T>A
ENST00000686801.1:c.4651T>A	ENSP00000509915.1:p.Tyr1551Asn
ENST00000686826.1:n.982T>A
ENST00000687016.1:c.4564T>A	ENSP00000509074.1:p.Tyr1522Asn
ENST00000687704.1:c.*2388T>A	ENSP00000510454.1:n.*2388T>A
ENST00000688066.1:c.4663T>A	ENSP00000510782.1:p.Tyr1555Asn
ENST00000688124.1:c.*3581T>A	ENSP00000510645.1:n.*3581T>A
ENST00000688848.1:c.*4007T>A	ENSP00000509419.1:n.*4007T>A
ENST00000688985.1:c.1664T>A	ENSP00000510477.1:n.1664T>A
ENST00000689129.1:c.4588T>A	ENSP00000510414.1:p.Tyr1530Asn
ENST00000689177.1:n.5935T>A
ENST00000689849.1:c.759T>A
ENST00000689981.1:c.4663T>A	ENSP00000509035.1:p.Tyr1555Asn
ENST00000690369.1:n.4681T>A
ENST00000690590.1:n.1710T>A
ENST00000690990.1:c.4657T>A	ENSP00000510461.1:p.Tyr1553Asn
ENST00000691233.1:c.4582T>A	ENSP00000509215.1:p.Tyr1528Asn
ENST00000691306.1:c.761T>A
ENST00000691345.1:n.2302+1182T>A
ENST00000691792.1:c.4651T>A	ENSP00000509911.1:p.Tyr1551Asn
ENST00000691959.1:n.5382T>A
ENST00000692844.1:n.1747T>A
ENST00000692946.1:c.759T>A
ENST00000693052.1:c.4681T>A	ENSP00000509558.1:p.Tyr1561Asn
ENST00000693289.1:n.1822T>A
ENST00000693440.1:c.4660T>A	ENSP00000509462.1:p.Tyr1554Asn
ENST00000693499.1:n.5588T>A
ENST00000693591.1:n.3400T>A
ENST00000380817.8:c.4663T>A MANE Select	ENSP00000370196.2:p.Tyr1555Asn
ENST00000348911.10:c.4588T>A	ENSP00000252027.7:p.Tyr1530Asn
ENST00000380817.7:c.4663T>A	ENSP00000370196.2:p.Tyr1555Asn
ENST00000418590.3:c.263T>A
ENST00000470434.1:n.804T>A
NM_002972.3:c.4663T>A	NP_002963.2:p.Tyr1555Asn
XM_005261931.1:c.4666T>A	XP_005261988.1:p.Tyr1556Asn
XM_005261935.1:c.4585T>A	XP_005261992.1:p.Tyr1529Asn
XM_011530707.1:c.4765T>A	XP_011529009.1:p.Tyr1589Asn
XM_011530708.1:c.4717T>A	XP_011529010.1:p.Tyr1573Asn
XM_011530709.1:c.4693T>A	XP_011529011.1:p.Tyr1565Asn
XM_011530710.1:c.4690T>A	XP_011529012.1:p.Tyr1564Asn
XM_011530711.1:c.4690T>A	XP_011529013.1:p.Tyr1564Asn
XR_938344.1:n.4783T>A
NM_001365819.1:c.4588T>A	NP_001352748.1:p.Tyr1530Asn
XM_005261935.2:c.4585T>A	XP_005261992.1:p.Tyr1529Asn
XM_011530709.2:c.4693T>A	XP_011529011.1:p.Tyr1565Asn
XM_011530710.2:c.4690T>A	XP_011529012.1:p.Tyr1564Asn
XM_017028905.2:c.4615T>A	XP_016884394.1:p.Tyr1539Asn
NM_002972.4:c.4663T>A MANE Select	NP_002963.2:p.Tyr1555Asn