Canonical Allele Identifier: CA412194055

Gene: SBF1

Linked Data

• MyVariant Identifiers: chr22:g.50893461A>T (hg19) ; chr22:g.50455032A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50455032A>T , CM000684.2:g.50455032A>T	GRCh38
NC_000022.10:g.50893461A>T , CM000684.1:g.50893461A>T	GRCh37
NC_000022.9:g.49240327A>T	NCBI36
NG_041810.1:g.25040T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.4587T>A	ENSP00000252027.8:p.Tyr1529Ter
ENST00000418590.4:c.297T>A	ENSP00000401538.2:p.Tyr99Ter
ENST00000470434.2:n.1068T>A
ENST00000684986.1:c.4668T>A	ENSP00000509117.1:p.Tyr1556Ter
ENST00000685180.1:n.2488+5502T>A
ENST00000685390.1:n.2633T>A
ENST00000685411.1:n.415T>A
ENST00000685592.1:c.899T>A
ENST00000685809.1:c.4578T>A	ENSP00000508863.1:p.Tyr1526Ter
ENST00000686029.1:c.743T>A
ENST00000686191.1:n.3865T>A
ENST00000686222.1:c.*4087T>A	ENSP00000508737.1:n.*4087T>A
ENST00000686321.1:c.761T>A
ENST00000686427.1:c.*1600T>A	ENSP00000510379.1:n.*1600T>A
ENST00000686758.1:n.2408T>A
ENST00000686801.1:c.4653T>A	ENSP00000509915.1:p.Tyr1551Ter
ENST00000686826.1:n.984T>A
ENST00000687016.1:c.4566T>A	ENSP00000509074.1:p.Tyr1522Ter
ENST00000687704.1:c.*2390T>A	ENSP00000510454.1:n.*2390T>A
ENST00000688066.1:c.4665T>A	ENSP00000510782.1:p.Tyr1555Ter
ENST00000688124.1:c.*3583T>A	ENSP00000510645.1:n.*3583T>A
ENST00000688848.1:c.*4009T>A	ENSP00000509419.1:n.*4009T>A
ENST00000688985.1:c.1666T>A	ENSP00000510477.1:n.1666T>A
ENST00000689129.1:c.4590T>A	ENSP00000510414.1:p.Tyr1530Ter
ENST00000689177.1:n.5937T>A
ENST00000689849.1:c.761T>A
ENST00000689981.1:c.4665T>A	ENSP00000509035.1:p.Tyr1555Ter
ENST00000690369.1:n.4683T>A
ENST00000690590.1:n.1712T>A
ENST00000690990.1:c.4659T>A	ENSP00000510461.1:p.Tyr1553Ter
ENST00000691233.1:c.4584T>A	ENSP00000509215.1:p.Tyr1528Ter
ENST00000691306.1:c.763T>A
ENST00000691345.1:n.2302+1184T>A
ENST00000691792.1:c.4653T>A	ENSP00000509911.1:p.Tyr1551Ter
ENST00000691959.1:n.5384T>A
ENST00000692844.1:n.1749T>A
ENST00000692946.1:c.761T>A
ENST00000693052.1:c.4683T>A	ENSP00000509558.1:p.Tyr1561Ter
ENST00000693289.1:n.1824T>A
ENST00000693440.1:c.4662T>A	ENSP00000509462.1:p.Tyr1554Ter
ENST00000693499.1:n.5590T>A
ENST00000693591.1:n.3402T>A
ENST00000380817.8:c.4665T>A MANE Select	ENSP00000370196.2:p.Tyr1555Ter
ENST00000348911.10:c.4590T>A	ENSP00000252027.7:p.Tyr1530Ter
ENST00000380817.7:c.4665T>A	ENSP00000370196.2:p.Tyr1555Ter
ENST00000418590.3:c.265T>A
ENST00000470434.1:n.806T>A
NM_002972.3:c.4665T>A	NP_002963.2:p.Tyr1555Ter
XM_005261931.1:c.4668T>A	XP_005261988.1:p.Tyr1556Ter
XM_005261935.1:c.4587T>A	XP_005261992.1:p.Tyr1529Ter
XM_011530707.1:c.4767T>A	XP_011529009.1:p.Tyr1589Ter
XM_011530708.1:c.4719T>A	XP_011529010.1:p.Tyr1573Ter
XM_011530709.1:c.4695T>A	XP_011529011.1:p.Tyr1565Ter
XM_011530710.1:c.4692T>A	XP_011529012.1:p.Tyr1564Ter
XM_011530711.1:c.4692T>A	XP_011529013.1:p.Tyr1564Ter
XR_938344.1:n.4785T>A
NM_001365819.1:c.4590T>A	NP_001352748.1:p.Tyr1530Ter
XM_005261935.2:c.4587T>A	XP_005261992.1:p.Tyr1529Ter
XM_011530709.2:c.4695T>A	XP_011529011.1:p.Tyr1565Ter
XM_011530710.2:c.4692T>A	XP_011529012.1:p.Tyr1564Ter
XM_017028905.2:c.4617T>A	XP_016884394.1:p.Tyr1539Ter
NM_002972.4:c.4665T>A MANE Select	NP_002963.2:p.Tyr1555Ter