Canonical Allele Identifier: CA2300141347

Gene: SETBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.44953288C= , CM000680.2:g.44953288C=	GRCh38
NC_000018.9:g.42533253C= , CM000680.1:g.42533253C=	GRCh37
NC_000018.8:g.40787251C=	NCBI36
NG_027527.1:g.278116C=
NG_027527.2:g.278116C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649279.2:c.3948C= MANE Select	ENSP00000497406.1:p.Ala1316=
ENST00000677068.1:c.3948C=	ENSP00000504398.1:p.Ala1316=
ENST00000677077.1:c.3948C=	ENSP00000503656.1:p.Ala1316=
ENST00000677130.1:c.3948C=	ENSP00000503094.1:p.Ala1316=
ENST00000677699.1:c.3948C=	ENSP00000503964.1:p.Ala1316=
ENST00000678152.1:c.3948C=	ENSP00000502995.1:p.Ala1316=
ENST00000282030.5:c.3948C=	ENSP00000282030.5:p.Ala1316=
NM_015559.2:c.3948C=	NP_056374.2:p.Ala1316=
XM_005258243.3:c.3948C=	XP_005258300.1:p.Ala1316=
NM_015559.3:c.3948C= MANE Select	NP_056374.2:p.Ala1316=
XM_024451149.1:c.4026C=	XP_024306917.1:p.Ala1342=
XM_024451150.1:c.4026C=	XP_024306918.1:p.Ala1342=
XM_024451151.1:c.4026C=	XP_024306919.1:p.Ala1342=
XM_024451152.1:c.4026C=	XP_024306920.1:p.Ala1342=
XM_024451153.1:c.3948C=	XP_024306921.1:p.Ala1316=
XM_024451154.1:c.3948C=	XP_024306922.1:p.Ala1316=
XM_024451155.1:c.3948C=	XP_024306923.1:p.Ala1316=
XM_024451156.1:c.4026C=	XP_024306924.1:p.Ala1342=
XM_024451157.1:c.3471C=	XP_024306925.1:p.Ala1157=
XM_024451158.1:c.4026C=	XP_024306926.1:p.Ala1342=
NM_001379141.1:c.3948C=	NP_001366070.1:p.Ala1316=
NM_001379142.1:c.3948C=	NP_001366071.1:p.Ala1316=