Canonical Allele Identifier: CA350387405

Gene: SATB2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199348819T>A , CM000664.2:g.199348819T>A	GRCh38
NC_000002.11:g.200213542T>A , CM000664.1:g.200213542T>A	GRCh37
NC_000002.10:g.199921787T>A	NCBI36
NG_016976.1:g.127448A>T
NG_016976.2:g.127448A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428695.6:c.701A>T	ENSP00000388581.1:p.Glu234Val
ENST00000700191.1:c.701A>T	ENSP00000514853.1:p.Glu234Val
ENST00000700193.1:c.1055A>T	ENSP00000514854.1:p.Glu352Val
ENST00000700208.1:c.347-76147A>T	ENSP00000514860.1:n.347-76147A>T
ENST00000700210.1:c.709A>T
ENST00000417098.6:c.1055A>T MANE Select	ENSP00000401112.1:p.Glu352Val
ENST00000260926.9:c.1055A>T	ENSP00000260926.5:p.Glu352Val
ENST00000417098.5:c.1055A>T	ENSP00000401112.1:p.Glu352Val
ENST00000428695.5:c.701A>T	ENSP00000388581.1:p.Glu234Val
ENST00000443023.5:c.878A>T	ENSP00000388764.1:p.Glu293Val
ENST00000457245.5:c.1055A>T	ENSP00000405420.1:p.Glu352Val
ENST00000483346.2:n.694A>T
ENST00000614512.4:c.701A>T	ENSP00000483287.1:p.Glu234Val
NM_001172509.1:c.1055A>T	NP_001165980.1:p.Glu352Val
NM_001172517.1:c.1055A>T	NP_001165988.1:p.Glu352Val
NM_015265.3:c.1055A>T	NP_056080.1:p.Glu352Val
XM_005246396.1:c.881A>T	XP_005246453.1:p.Glu294Val
XM_006712372.1:c.1055A>T	XP_006712435.1:p.Glu352Val
XM_011510840.1:c.1055A>T	XP_011509142.1:p.Glu352Val
XM_005246396.3:c.881A>T	XP_005246453.1:p.Glu294Val
XM_011510840.3:c.1055A>T	XP_011509142.1:p.Glu352Val
XM_017003656.1:c.881A>T	XP_016859145.1:p.Glu294Val
XM_024452767.1:c.632A>T	XP_024308535.1:p.Glu211Val
XM_024452768.1:c.632A>T	XP_024308536.1:p.Glu211Val
NM_001172509.2:c.1055A>T MANE Select	NP_001165980.1:p.Glu352Val
NM_015265.4:c.1055A>T	NP_056080.1:p.Glu352Val