Canonical Allele Identifier: CA1320151659

Gene: SATB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199348835T= , CM000664.2:g.199348835T=	GRCh38
NC_000002.11:g.200213558T= , CM000664.1:g.200213558T=	GRCh37
NC_000002.10:g.199921803T=	NCBI36
NG_016976.1:g.127432A=
NG_016976.2:g.127432A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428695.6:c.685A=	ENSP00000388581.1:p.Arg229=
ENST00000700191.1:c.685A=	ENSP00000514853.1:p.Arg229=
ENST00000700193.1:c.1039A=	ENSP00000514854.1:p.Arg347=
ENST00000700208.1:c.347-76163A=	ENSP00000514860.1:n.347-76163A=
ENST00000700210.1:c.693A=
ENST00000417098.6:c.1039A= MANE Select	ENSP00000401112.1:p.Arg347=
ENST00000260926.9:c.1039A=	ENSP00000260926.5:p.Arg347=
ENST00000417098.5:c.1039A=	ENSP00000401112.1:p.Arg347=
ENST00000428695.5:c.685A=	ENSP00000388581.1:p.Arg229=
ENST00000443023.5:c.862A=	ENSP00000388764.1:p.Arg288=
ENST00000457245.5:c.1039A=	ENSP00000405420.1:p.Arg347=
ENST00000483346.2:n.678A=
ENST00000614512.4:c.685A=	ENSP00000483287.1:p.Arg229=
NM_001172509.1:c.1039A=	NP_001165980.1:p.Arg347=
NM_001172517.1:c.1039A=	NP_001165988.1:p.Arg347=
NM_015265.3:c.1039A=	NP_056080.1:p.Arg347=
XM_005246396.1:c.865A=	XP_005246453.1:p.Arg289=
XM_006712372.1:c.1039A=	XP_006712435.1:p.Arg347=
XM_011510840.1:c.1039A=	XP_011509142.1:p.Arg347=
XM_005246396.3:c.865A=	XP_005246453.1:p.Arg289=
XM_011510840.3:c.1039A=	XP_011509142.1:p.Arg347=
XM_017003656.1:c.865A=	XP_016859145.1:p.Arg289=
XM_024452767.1:c.616A=	XP_024308535.1:p.Arg206=
XM_024452768.1:c.616A=	XP_024308536.1:p.Arg206=
NM_001172509.2:c.1039A= MANE Select	NP_001165980.1:p.Arg347=
NM_015265.4:c.1039A=	NP_056080.1:p.Arg347=