Canonical Allele Identifier: CA10641476

Gene: SETBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45066668_45066669insT , CM000680.2:g.45066668_45066669insT	GRCh38
NC_000018.9:g.42646633_42646634insT , CM000680.1:g.42646633_42646634insT	GRCh37
NC_000018.8:g.40900631_40900632insT	NCBI36
NG_027527.1:g.391496_391497insT
NG_027527.2:g.391496_391497insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649279.2:c.*2970_*2971insT MANE Select	ENSP00000497406.1:n.*2970_*2971insT
ENST00000677077.1:c.*2970_*2971insT	ENSP00000503656.1:n.*2970_*2971insT
ENST00000677130.1:c.*2970_*2971insT	ENSP00000503094.1:n.*2970_*2971insT
ENST00000677699.1:c.*2970_*2971insT	ENSP00000503964.1:n.*2970_*2971insT
ENST00000678152.1:c.*2970_*2971insT	ENSP00000502995.1:n.*2970_*2971insT
ENST00000282030.5:c.*2970_*2971insT	ENSP00000282030.5:n.*2970_*2971insT
NM_015559.2:c.*2970_*2971insT	NP_056374.2:n.*2970_*2971insT
XM_005258243.3:c.*2970_*2971insT	XP_005258300.1:n.*2970_*2971insT
NM_015559.3:c.*2970_*2971insT MANE Select	NP_056374.2:n.*2970_*2971insT
XM_024451149.1:c.*2970_*2971insT	XP_024306917.1:n.*2970_*2971insT
XM_024451150.1:c.*2970_*2971insT	XP_024306918.1:n.*2970_*2971insT
XM_024451151.1:c.*2970_*2971insT	XP_024306919.1:n.*2970_*2971insT
XM_024451152.1:c.*2970_*2971insT	XP_024306920.1:n.*2970_*2971insT
XM_024451153.1:c.*2970_*2971insT	XP_024306921.1:n.*2970_*2971insT
XM_024451154.1:c.*2970_*2971insT	XP_024306922.1:n.*2970_*2971insT
XM_024451155.1:c.*2970_*2971insT	XP_024306923.1:n.*2970_*2971insT
XM_024451156.1:c.*2970_*2971insT	XP_024306924.1:n.*2970_*2971insT
XM_024451157.1:c.*2970_*2971insT	XP_024306925.1:n.*2970_*2971insT
NM_001379141.1:c.*2970_*2971insT	NP_001366070.1:n.*2970_*2971insT
NM_001379142.1:c.*2970_*2971insT	NP_001366071.1:n.*2970_*2971insT