Canonical Allele Identifier: CA1320151670

Gene: SATB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199348874C= , CM000664.2:g.199348874C=	GRCh38
NC_000002.11:g.200213597C= , CM000664.1:g.200213597C=	GRCh37
NC_000002.10:g.199921842C=	NCBI36
NG_016976.1:g.127393G=
NG_016976.2:g.127393G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428695.6:c.646G=	ENSP00000388581.1:p.Ala216=
ENST00000700191.1:c.646G=	ENSP00000514853.1:p.Ala216=
ENST00000700193.1:c.1000G=	ENSP00000514854.1:p.Ala334=
ENST00000700208.1:c.347-76202G=	ENSP00000514860.1:n.347-76202G=
ENST00000700210.1:c.654G=
ENST00000417098.6:c.1000G= MANE Select	ENSP00000401112.1:p.Ala334=
ENST00000260926.9:c.1000G=	ENSP00000260926.5:p.Ala334=
ENST00000417098.5:c.1000G=	ENSP00000401112.1:p.Ala334=
ENST00000428695.5:c.646G=	ENSP00000388581.1:p.Ala216=
ENST00000443023.5:c.823G=	ENSP00000388764.1:p.Ala275=
ENST00000457245.5:c.1000G=	ENSP00000405420.1:p.Ala334=
ENST00000483346.2:n.639G=
ENST00000614512.4:c.646G=	ENSP00000483287.1:p.Ala216=
NM_001172509.1:c.1000G=	NP_001165980.1:p.Ala334=
NM_001172517.1:c.1000G=	NP_001165988.1:p.Ala334=
NM_015265.3:c.1000G=	NP_056080.1:p.Ala334=
XM_005246396.1:c.826G=	XP_005246453.1:p.Ala276=
XM_006712372.1:c.1000G=	XP_006712435.1:p.Ala334=
XM_011510840.1:c.1000G=	XP_011509142.1:p.Ala334=
XM_005246396.3:c.826G=	XP_005246453.1:p.Ala276=
XM_011510840.3:c.1000G=	XP_011509142.1:p.Ala334=
XM_017003656.1:c.826G=	XP_016859145.1:p.Ala276=
XM_024452767.1:c.577G=	XP_024308535.1:p.Ala193=
XM_024452768.1:c.577G=	XP_024308536.1:p.Ala193=
NM_001172509.2:c.1000G= MANE Select	NP_001165980.1:p.Ala334=
NM_015265.4:c.1000G=	NP_056080.1:p.Ala334=