Canonical Allele Identifier: CA1320194416

Gene: SATB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199455830G= , CM000664.2:g.199455830G=	GRCh38
NC_000002.11:g.200320553G= , CM000664.1:g.200320553G=	GRCh37
NC_000002.10:g.200028798G=	NCBI36
NG_016976.1:g.20437C=
NG_016976.2:g.20437C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428695.6:c.169+39C=	ENSP00000388581.1:n.169+39C=
ENST00000700191.1:c.169+39C=	ENSP00000514853.1:n.169+39C=
ENST00000700193.1:c.169+39C=	ENSP00000514854.1:n.169+39C=
ENST00000700194.1:n.427+39C=
ENST00000700208.1:c.169+39C=	ENSP00000514860.1:n.169+39C=
ENST00000417098.6:c.169+39C= MANE Select	ENSP00000401112.1:n.169+39C=
ENST00000260926.9:c.169+39C=	ENSP00000260926.5:n.169+39C=
ENST00000417098.5:c.169+39C=	ENSP00000401112.1:n.169+39C=
ENST00000428695.5:c.169+39C=	ENSP00000388581.1:n.169+39C=
ENST00000440919.1:c.169+39C=	ENSP00000415610.1:n.169+39C=
ENST00000443023.5:c.169+39C=	ENSP00000388764.1:n.169+39C=
ENST00000457245.5:c.169+39C=	ENSP00000405420.1:n.169+39C=
ENST00000614512.4:c.169+39C=	ENSP00000483287.1:n.169+39C=
NM_001172509.1:c.169+39C=	NP_001165980.1:n.169+39C=
NM_001172517.1:c.169+39C=	NP_001165988.1:n.169+39C=
NM_015265.3:c.169+39C=	NP_056080.1:n.169+39C=
XM_005246396.1:c.-6+4622C=	XP_005246453.1:n.-6+4622C=
XM_006712372.1:c.169+39C=	XP_006712435.1:n.169+39C=
XM_011510840.1:c.169+39C=	XP_011509142.1:n.169+39C=
NR_134967.1:n.986+39C=
XM_005246396.3:c.-6+4622C=	XP_005246453.1:n.-6+4622C=
XM_011510840.3:c.169+39C=	XP_011509142.1:n.169+39C=
XM_017003656.1:c.-6+4622C=	XP_016859145.1:n.-6+4622C=
NM_001172509.2:c.169+39C= MANE Select	NP_001165980.1:n.169+39C=
NM_015265.4:c.169+39C=	NP_056080.1:n.169+39C=
NR_134967.2:n.829+39C=