Canonical Allele Identifier: CA350388525
Gene: SATB2 HGNC NCBI

Linked Data

dbSNP Id: rs1559066045

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.199455956G>C , CM000664.2:g.199455956G>C GRCh38
NC_000002.11:g.200320679G>C , CM000664.1:g.200320679G>C GRCh37
NC_000002.10:g.200028924G>C NCBI36
NG_016976.1:g.20311C>G
NG_016976.2:g.20311C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000428695.6:c.82C>G ENSP00000388581.1:p.Pro28Ala
ENST00000700191.1:c.82C>G ENSP00000514853.1:p.Pro28Ala
ENST00000700193.1:c.82C>G ENSP00000514854.1:p.Pro28Ala
ENST00000700194.1:n.340C>G
ENST00000700208.1:c.82C>G ENSP00000514860.1:p.Pro28Ala
ENST00000417098.6:c.82C>G MANE Select ENSP00000401112.1:p.Pro28Ala
ENST00000260926.9:c.82C>G ENSP00000260926.5:p.Pro28Ala
ENST00000417098.5:c.82C>G ENSP00000401112.1:p.Pro28Ala
ENST00000428695.5:c.82C>G ENSP00000388581.1:p.Pro28Ala
ENST00000440919.1:c.82C>G ENSP00000415610.1:p.Pro28Ala
ENST00000443023.5:c.82C>G ENSP00000388764.1:p.Pro28Ala
ENST00000457245.5:c.82C>G ENSP00000405420.1:p.Pro28Ala
ENST00000614512.4:c.82C>G ENSP00000483287.1:p.Pro28Ala
NM_001172509.1:c.82C>G NP_001165980.1:p.Pro28Ala
NM_001172517.1:c.82C>G NP_001165988.1:p.Pro28Ala
NM_015265.3:c.82C>G NP_056080.1:p.Pro28Ala
XM_005246396.1:c.-6+4496C>G XP_005246453.1:n.-6+4496C>G
XM_006712372.1:c.82C>G XP_006712435.1:p.Pro28Ala
XM_011510840.1:c.82C>G XP_011509142.1:p.Pro28Ala
NR_134967.1:n.899C>G
XM_005246396.3:c.-6+4496C>G XP_005246453.1:n.-6+4496C>G
XM_011510840.3:c.82C>G XP_011509142.1:p.Pro28Ala
XM_017003656.1:c.-6+4496C>G XP_016859145.1:n.-6+4496C>G
NM_001172509.2:c.82C>G MANE Select NP_001165980.1:p.Pro28Ala
NM_015265.4:c.82C>G NP_056080.1:p.Pro28Ala
NR_134967.2:n.742C>G