Canonical Allele Identifier: CA2831901197

Gene: SETBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.44798368_44798369insCCCC , CM000680.2:g.44798368_44798369insCCCC	GRCh38
NC_000018.9:g.42378333_42378334insCCCC , CM000680.1:g.42378333_42378334insCCCC	GRCh37
NC_000018.8:g.40632331_40632332insCCCC	NCBI36
NG_027527.1:g.123196_123197insCCCC
NG_027527.2:g.123196_123197insCCCC

Transcript Alleles

HGVS	Amino-acid Change
NM_015559.3:c.487-70862_487-70861insCCCC MANE Select	NP_056374.2:n.487-70862_487-70861insCCCC
ENST00000649279.2:c.487-70862_487-70861insCCCC MANE Select	ENSP00000497406.1:n.487-70862_487-70861insCCCC
NM_001130110.1:c.487-70862_487-70861insCCCC	NP_001123582.1:n.487-70862_487-70861insCCCC
NM_001130110.2:c.487-70862_487-70861insCCCC	NP_001123582.1:n.487-70862_487-70861insCCCC
NM_001379141.1:c.487-70862_487-70861insCCCC	NP_001366070.1:n.487-70862_487-70861insCCCC
NM_001379142.1:c.487-70862_487-70861insCCCC	NP_001366071.1:n.487-70862_487-70861insCCCC
NM_015559.2:c.487-70862_487-70861insCCCC	NP_056374.2:n.487-70862_487-70861insCCCC
ENST00000282030.5:c.487-70862_487-70861insCCCC	ENSP00000282030.5:n.487-70862_487-70861insCCCC
ENST00000426838.8:c.487-70862_487-70861insCCCC	ENSP00000390687.3:n.487-70862_487-70861insCCCC
ENST00000645568.1:c.487-70862_487-70861insCCCC	ENSP00000496513.1:n.487-70862_487-70861insCCCC
ENST00000677068.1:c.487-70862_487-70861insCCCC	ENSP00000504398.1:n.487-70862_487-70861insCCCC
ENST00000677077.1:c.487-70862_487-70861insCCCC	ENSP00000503656.1:n.487-70862_487-70861insCCCC
ENST00000677130.1:c.487-70862_487-70861insCCCC	ENSP00000503094.1:n.487-70862_487-70861insCCCC
ENST00000677699.1:c.487-70862_487-70861insCCCC	ENSP00000503964.1:n.487-70862_487-70861insCCCC
ENST00000678152.1:c.487-70862_487-70861insCCCC	ENSP00000502995.1:n.487-70862_487-70861insCCCC
XM_005258243.3:c.487-70862_487-70861insCCCC	XP_005258300.1:n.487-70862_487-70861insCCCC
XM_024451149.1:c.565-70862_565-70861insCCCC	XP_024306917.1:n.565-70862_565-70861insCCCC
XM_024451150.1:c.565-70862_565-70861insCCCC	XP_024306918.1:n.565-70862_565-70861insCCCC
XM_024451151.1:c.565-70862_565-70861insCCCC	XP_024306919.1:n.565-70862_565-70861insCCCC
XM_024451152.1:c.565-70862_565-70861insCCCC	XP_024306920.1:n.565-70862_565-70861insCCCC
XM_024451153.1:c.487-70862_487-70861insCCCC	XP_024306921.1:n.487-70862_487-70861insCCCC
XM_024451154.1:c.487-70862_487-70861insCCCC	XP_024306922.1:n.487-70862_487-70861insCCCC
XM_024451155.1:c.487-70862_487-70861insCCCC	XP_024306923.1:n.487-70862_487-70861insCCCC
XM_024451156.1:c.565-70862_565-70861insCCCC	XP_024306924.1:n.565-70862_565-70861insCCCC
XM_024451157.1:c.-1915_-1914insCCCC	XP_024306925.1:n.-1915_-1914insCCCC
XM_024451158.1:c.565-70862_565-70861insCCCC	XP_024306926.1:n.565-70862_565-70861insCCCC
XR_935419.1:n.1120-1622_1120-1621insCCCC