Canonical Allele Identifier: CA1320184577
Gene: SATB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.199433402G= , CM000664.2:g.199433402G= GRCh38
NC_000002.11:g.200298125G= , CM000664.1:g.200298125G= GRCh37
NC_000002.10:g.200006370G= NCBI36
NG_016976.1:g.42865C=
NG_016976.2:g.42865C=

Transcript Alleles

HGVS Amino-acid change
ENST00000428695.6:c.282C= ENSP00000388581.1:p.Ser94=
ENST00000700191.1:c.282C= ENSP00000514853.1:p.Ser94=
ENST00000700193.1:c.282C= ENSP00000514854.1:p.Ser94=
ENST00000700194.1:n.540C=
ENST00000700208.1:c.282C= ENSP00000514860.1:p.Ser94=
ENST00000417098.6:c.282C= MANE Select ENSP00000401112.1:p.Ser94=
ENST00000260926.9:c.282C= ENSP00000260926.5:p.Ser94=
ENST00000417098.5:c.282C= ENSP00000401112.1:p.Ser94=
ENST00000428695.5:c.282C= ENSP00000388581.1:p.Ser94=
ENST00000440919.1:c.282C= ENSP00000415610.1:p.Ser94=
ENST00000443023.5:c.169+22467C= ENSP00000388764.1:n.169+22467C=
ENST00000457245.5:c.282C= ENSP00000405420.1:p.Ser94=
ENST00000614512.4:c.282C= ENSP00000483287.1:p.Ser94=
NM_001172509.1:c.282C= NP_001165980.1:p.Ser94=
NM_001172517.1:c.282C= NP_001165988.1:p.Ser94=
NM_015265.3:c.282C= NP_056080.1:p.Ser94=
XM_005246396.1:c.108C= XP_005246453.1:p.Ser36=
XM_006712372.1:c.282C= XP_006712435.1:p.Ser94=
XM_011510840.1:c.282C= XP_011509142.1:p.Ser94=
NR_134967.1:n.1099C=
XM_005246396.3:c.108C= XP_005246453.1:p.Ser36=
XM_011510840.3:c.282C= XP_011509142.1:p.Ser94=
XM_017003656.1:c.108C= XP_016859145.1:p.Ser36=
XM_024452767.1:c.-352C= XP_024308535.1:n.-352C=
NM_001172509.2:c.282C= MANE Select NP_001165980.1:p.Ser94=
NM_015265.4:c.282C= NP_056080.1:p.Ser94=
NR_134967.2:n.942C=