Canonical Allele Identifier: CA1320151666

Gene: SATB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199348862G= , CM000664.2:g.199348862G=	GRCh38
NC_000002.11:g.200213585G= , CM000664.1:g.200213585G=	GRCh37
NC_000002.10:g.199921830G=	NCBI36
NG_016976.1:g.127405C=
NG_016976.2:g.127405C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428695.6:c.658C=	ENSP00000388581.1:p.Gln220=
ENST00000700191.1:c.658C=	ENSP00000514853.1:p.Gln220=
ENST00000700193.1:c.1012C=	ENSP00000514854.1:p.Gln338=
ENST00000700208.1:c.347-76190C=	ENSP00000514860.1:n.347-76190C=
ENST00000700210.1:c.666C=
ENST00000417098.6:c.1012C= MANE Select	ENSP00000401112.1:p.Gln338=
ENST00000260926.9:c.1012C=	ENSP00000260926.5:p.Gln338=
ENST00000417098.5:c.1012C=	ENSP00000401112.1:p.Gln338=
ENST00000428695.5:c.658C=	ENSP00000388581.1:p.Gln220=
ENST00000443023.5:c.835C=	ENSP00000388764.1:p.Gln279=
ENST00000457245.5:c.1012C=	ENSP00000405420.1:p.Gln338=
ENST00000483346.2:n.651C=
ENST00000614512.4:c.658C=	ENSP00000483287.1:p.Gln220=
NM_001172509.1:c.1012C=	NP_001165980.1:p.Gln338=
NM_001172517.1:c.1012C=	NP_001165988.1:p.Gln338=
NM_015265.3:c.1012C=	NP_056080.1:p.Gln338=
XM_005246396.1:c.838C=	XP_005246453.1:p.Gln280=
XM_006712372.1:c.1012C=	XP_006712435.1:p.Gln338=
XM_011510840.1:c.1012C=	XP_011509142.1:p.Gln338=
XM_005246396.3:c.838C=	XP_005246453.1:p.Gln280=
XM_011510840.3:c.1012C=	XP_011509142.1:p.Gln338=
XM_017003656.1:c.838C=	XP_016859145.1:p.Gln280=
XM_024452767.1:c.589C=	XP_024308535.1:p.Gln197=
XM_024452768.1:c.589C=	XP_024308536.1:p.Gln197=
NM_001172509.2:c.1012C= MANE Select	NP_001165980.1:p.Gln338=
NM_015265.4:c.1012C=	NP_056080.1:p.Gln338=