Canonical Allele Identifier: CA1320151703

Gene: SATB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199348995C= , CM000664.2:g.199348995C=	GRCh38
NC_000002.11:g.200213718C= , CM000664.1:g.200213718C=	GRCh37
NC_000002.10:g.199921963C=	NCBI36
NG_016976.1:g.127272G=
NG_016976.2:g.127272G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428695.6:c.525G=	ENSP00000388581.1:p.Met175=
ENST00000700191.1:c.525G=	ENSP00000514853.1:p.Met175=
ENST00000700193.1:c.879G=	ENSP00000514854.1:p.Met293=
ENST00000700208.1:c.347-76323G=	ENSP00000514860.1:n.347-76323G=
ENST00000700210.1:c.533G=
ENST00000417098.6:c.879G= MANE Select	ENSP00000401112.1:p.Met293=
ENST00000260926.9:c.879G=	ENSP00000260926.5:p.Met293=
ENST00000417098.5:c.879G=	ENSP00000401112.1:p.Met293=
ENST00000428695.5:c.525G=	ENSP00000388581.1:p.Met175=
ENST00000443023.5:c.702G=	ENSP00000388764.1:p.Met234=
ENST00000457245.5:c.879G=	ENSP00000405420.1:p.Met293=
ENST00000483346.2:n.518G=
ENST00000614512.4:c.525G=	ENSP00000483287.1:p.Met175=
NM_001172509.1:c.879G=	NP_001165980.1:p.Met293=
NM_001172517.1:c.879G=	NP_001165988.1:p.Met293=
NM_015265.3:c.879G=	NP_056080.1:p.Met293=
XM_005246396.1:c.705G=	XP_005246453.1:p.Met235=
XM_006712372.1:c.879G=	XP_006712435.1:p.Met293=
XM_011510840.1:c.879G=	XP_011509142.1:p.Met293=
XM_005246396.3:c.705G=	XP_005246453.1:p.Met235=
XM_011510840.3:c.879G=	XP_011509142.1:p.Met293=
XM_017003656.1:c.705G=	XP_016859145.1:p.Met235=
XM_024452767.1:c.456G=	XP_024308535.1:p.Met152=
XM_024452768.1:c.456G=	XP_024308536.1:p.Met152=
NM_001172509.2:c.879G= MANE Select	NP_001165980.1:p.Met293=
NM_015265.4:c.879G=	NP_056080.1:p.Met293=