Canonical Allele Identifier: CA1320194424

Gene: SATB2

Linked Data

• dbSNP Id: rs1692256415

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199455846_199455847dup , CM000664.2:g.199455846_199455847dup	GRCh38
NC_000002.11:g.200320569_200320570dup , CM000664.1:g.200320569_200320570dup	GRCh37
NC_000002.10:g.200028814_200028815dup	NCBI36
NG_016976.1:g.20424_20425dup
NG_016976.2:g.20424_20425dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428695.6:c.169+26_169+27dup	ENSP00000388581.1:n.169+26_169+27dup
ENST00000700191.1:c.169+26_169+27dup	ENSP00000514853.1:n.169+26_169+27dup
ENST00000700193.1:c.169+26_169+27dup	ENSP00000514854.1:n.169+26_169+27dup
ENST00000700194.1:n.427+26_427+27dup
ENST00000700208.1:c.169+26_169+27dup	ENSP00000514860.1:n.169+26_169+27dup
ENST00000417098.6:c.169+26_169+27dup MANE Select	ENSP00000401112.1:n.169+26_169+27dup
ENST00000260926.9:c.169+26_169+27dup	ENSP00000260926.5:n.169+26_169+27dup
ENST00000417098.5:c.169+26_169+27dup	ENSP00000401112.1:n.169+26_169+27dup
ENST00000428695.5:c.169+26_169+27dup	ENSP00000388581.1:n.169+26_169+27dup
ENST00000440919.1:c.169+26_169+27dup	ENSP00000415610.1:n.169+26_169+27dup
ENST00000443023.5:c.169+26_169+27dup	ENSP00000388764.1:n.169+26_169+27dup
ENST00000457245.5:c.169+26_169+27dup	ENSP00000405420.1:n.169+26_169+27dup
ENST00000614512.4:c.169+26_169+27dup	ENSP00000483287.1:n.169+26_169+27dup
NM_001172509.1:c.169+26_169+27dup	NP_001165980.1:n.169+26_169+27dup
NM_001172517.1:c.169+26_169+27dup	NP_001165988.1:n.169+26_169+27dup
NM_015265.3:c.169+26_169+27dup	NP_056080.1:n.169+26_169+27dup
XM_005246396.1:c.-6+4609_-6+4610dup	XP_005246453.1:n.-6+4609_-6+4610dup
XM_006712372.1:c.169+26_169+27dup	XP_006712435.1:n.169+26_169+27dup
XM_011510840.1:c.169+26_169+27dup	XP_011509142.1:n.169+26_169+27dup
NR_134967.1:n.986+26_986+27dup
XM_005246396.3:c.-6+4609_-6+4610dup	XP_005246453.1:n.-6+4609_-6+4610dup
XM_011510840.3:c.169+26_169+27dup	XP_011509142.1:n.169+26_169+27dup
XM_017003656.1:c.-6+4609_-6+4610dup	XP_016859145.1:n.-6+4609_-6+4610dup
NM_001172509.2:c.169+26_169+27dup MANE Select	NP_001165980.1:n.169+26_169+27dup
NM_015265.4:c.169+26_169+27dup	NP_056080.1:n.169+26_169+27dup
NR_134967.2:n.829+26_829+27dup