Canonical Allele Identifier: CA1320151693

Gene: SATB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199348968A= , CM000664.2:g.199348968A=	GRCh38
NC_000002.11:g.200213691A= , CM000664.1:g.200213691A=	GRCh37
NC_000002.10:g.199921936A=	NCBI36
NG_016976.1:g.127299T=
NG_016976.2:g.127299T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428695.6:c.552T=	ENSP00000388581.1:p.Leu184=
ENST00000700191.1:c.552T=	ENSP00000514853.1:p.Leu184=
ENST00000700193.1:c.906T=	ENSP00000514854.1:p.Leu302=
ENST00000700208.1:c.347-76296T=	ENSP00000514860.1:n.347-76296T=
ENST00000700210.1:c.560T=
ENST00000417098.6:c.906T= MANE Select	ENSP00000401112.1:p.Leu302=
ENST00000260926.9:c.906T=	ENSP00000260926.5:p.Leu302=
ENST00000417098.5:c.906T=	ENSP00000401112.1:p.Leu302=
ENST00000428695.5:c.552T=	ENSP00000388581.1:p.Leu184=
ENST00000443023.5:c.729T=	ENSP00000388764.1:p.Leu243=
ENST00000457245.5:c.906T=	ENSP00000405420.1:p.Leu302=
ENST00000483346.2:n.545T=
ENST00000614512.4:c.552T=	ENSP00000483287.1:p.Leu184=
NM_001172509.1:c.906T=	NP_001165980.1:p.Leu302=
NM_001172517.1:c.906T=	NP_001165988.1:p.Leu302=
NM_015265.3:c.906T=	NP_056080.1:p.Leu302=
XM_005246396.1:c.732T=	XP_005246453.1:p.Leu244=
XM_006712372.1:c.906T=	XP_006712435.1:p.Leu302=
XM_011510840.1:c.906T=	XP_011509142.1:p.Leu302=
XM_005246396.3:c.732T=	XP_005246453.1:p.Leu244=
XM_011510840.3:c.906T=	XP_011509142.1:p.Leu302=
XM_017003656.1:c.732T=	XP_016859145.1:p.Leu244=
XM_024452767.1:c.483T=	XP_024308535.1:p.Leu161=
XM_024452768.1:c.483T=	XP_024308536.1:p.Leu161=
NM_001172509.2:c.906T= MANE Select	NP_001165980.1:p.Leu302=
NM_015265.4:c.906T=	NP_056080.1:p.Leu302=