Canonical Allele Identifier: CA2300140775
Gene: SETBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.44951923T= , CM000680.2:g.44951923T= GRCh38
NC_000018.9:g.42531888T= , CM000680.1:g.42531888T= GRCh37
NC_000018.8:g.40785886T= NCBI36
NG_027527.1:g.276751T=
NG_027527.2:g.276751T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649279.2:c.2583T= MANE Select ENSP00000497406.1:p.Ser861=
ENST00000677068.1:c.2583T= ENSP00000504398.1:p.Ser861=
ENST00000677077.1:c.2583T= ENSP00000503656.1:p.Ser861=
ENST00000677130.1:c.2583T= ENSP00000503094.1:p.Ser861=
ENST00000677699.1:c.2583T= ENSP00000503964.1:p.Ser861=
ENST00000678152.1:c.2583T= ENSP00000502995.1:p.Ser861=
ENST00000282030.5:c.2583T= ENSP00000282030.5:p.Ser861=
NM_015559.2:c.2583T= NP_056374.2:p.Ser861=
XM_005258243.3:c.2583T= XP_005258300.1:p.Ser861=
NM_015559.3:c.2583T= MANE Select NP_056374.2:p.Ser861=
XM_024451149.1:c.2661T= XP_024306917.1:p.Ser887=
XM_024451150.1:c.2661T= XP_024306918.1:p.Ser887=
XM_024451151.1:c.2661T= XP_024306919.1:p.Ser887=
XM_024451152.1:c.2661T= XP_024306920.1:p.Ser887=
XM_024451153.1:c.2583T= XP_024306921.1:p.Ser861=
XM_024451154.1:c.2583T= XP_024306922.1:p.Ser861=
XM_024451155.1:c.2583T= XP_024306923.1:p.Ser861=
XM_024451156.1:c.2661T= XP_024306924.1:p.Ser887=
XM_024451157.1:c.2106T= XP_024306925.1:p.Ser702=
XM_024451158.1:c.2661T= XP_024306926.1:p.Ser887=
NM_001379141.1:c.2583T= NP_001366070.1:p.Ser861=
NM_001379142.1:c.2583T= NP_001366071.1:p.Ser861=