Canonical Allele Identifier: CA379645819
Community Standard Title: NM_030962.4(SBF2):c.613C>T (p.Gln205Ter)
Gene: SBF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10028458G>A , CM000673.2:g.10028458G>A GRCh38
NC_000011.9:g.10050005G>A , CM000673.1:g.10050005G>A GRCh37
NC_000011.8:g.10006581G>A NCBI36
NG_008074.1:g.270750C>T , LRG_267:g.270750C>T

Transcript Alleles

HGVS Amino-acid Change
NM_030962.4:c.613C>T MANE Select NP_112224.1:p.Gln205Ter
ENST00000256190.13:c.613C>T MANE Select ENSP00000256190.8:p.Gln205Ter
NM_001386339.1:c.613C>T NP_001373268.1:p.Gln205Ter
NM_001386342.1:c.613C>T NP_001373271.1:p.Gln205Ter
NM_030962.3:c.613C>T , LRG_267t1:c.613C>T NP_112224.1:p.Gln205Ter
ENST00000256190.12:c.613C>T ENSP00000256190.8:p.Gln205Ter
ENST00000526353.2:n.763C>T
ENST00000527019.5:n.560C>T
ENST00000527019.6:n.560C>T
ENST00000533661.1:n.481C>T
ENST00000533661.2:n.569C>T
ENST00000533770.5:n.528C>T
ENST00000533770.6:c.613C>T ENSP00000509247.1:p.Gln205Ter
ENST00000617179.4:c.472C>T ENSP00000482806.1:p.Gln158Ter
ENST00000675281.1:c.613C>T ENSP00000502491.1:p.Gln205Ter
ENST00000675281.2:c.613C>T ENSP00000502491.1:p.Gln205Ter
ENST00000676324.1:c.613C>T ENSP00000502578.1:p.Gln205Ter
ENST00000676324.2:c.613C>T ENSP00000502578.1:p.Gln205Ter
ENST00000676387.1:c.613C>T ENSP00000502779.1:p.Gln205Ter
ENST00000676387.2:c.613C>T ENSP00000502779.1:p.Gln205Ter
ENST00000685217.1:n.944C>T
ENST00000686079.1:c.613C>T ENSP00000509599.1:p.Gln205Ter
ENST00000687210.1:c.613C>T ENSP00000509480.1:p.Gln205Ter
ENST00000687256.1:c.613C>T ENSP00000508741.1:p.Gln205Ter
ENST00000687300.1:c.613C>T ENSP00000508415.1:p.Gln205Ter
ENST00000688206.1:c.613C>T ENSP00000510516.1:p.Gln205Ter
ENST00000688344.1:c.334C>T ENSP00000509987.1:p.Gln112Ter
ENST00000688417.1:n.763C>T
ENST00000689128.1:c.613C>T ENSP00000509587.1:p.Gln205Ter
ENST00000689258.1:c.475C>T ENSP00000510475.1:p.Gln159Ter
ENST00000689940.1:c.613C>T ENSP00000508452.1:p.Gln205Ter
ENST00000692716.1:c.613C>T ENSP00000509545.1:p.Gln205Ter
ENST00000693022.1:c.613C>T ENSP00000508914.1:p.Gln205Ter
ENST00000693201.1:c.*195C>T ENSP00000510346.1:n.*195C>T
ENST00000693212.1:c.613C>T ENSP00000510716.1:p.Gln205Ter
XM_005253154.3:c.613C>T XP_005253211.1:p.Gln205Ter
XM_005253154.5:c.613C>T XP_005253211.1:p.Gln205Ter
XM_005253155.3:c.613C>T XP_005253212.1:p.Gln205Ter
XM_005253155.5:c.613C>T XP_005253212.1:p.Gln205Ter
XM_011520394.1:c.613C>T XP_011518696.1:p.Gln205Ter
XM_011520394.3:c.613C>T XP_011518696.1:p.Gln205Ter
XM_011520395.1:c.613C>T XP_011518697.1:p.Gln205Ter
XM_011520395.3:c.613C>T XP_011518697.1:p.Gln205Ter
XM_011520396.1:c.613C>T XP_011518698.1:p.Gln205Ter
XM_011520396.3:c.613C>T XP_011518698.1:p.Gln205Ter
XM_017018372.2:c.475C>T XP_016873861.1:p.Gln159Ter
XM_017018373.2:c.475C>T XP_016873862.1:p.Gln159Ter
XM_017018374.2:c.613C>T XP_016873863.1:p.Gln205Ter
XM_017018375.2:c.613C>T XP_016873864.1:p.Gln205Ter
XM_017018376.2:c.613C>T XP_016873865.1:p.Gln205Ter
XM_017018377.2:c.613C>T XP_016873866.1:p.Gln205Ter
XR_001747994.2:n.751C>T