Canonical Allele Identifier: CA1320151696

Gene: SATB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199348978_199348979delinsGA , CM000664.2:g.199348978_199348979delinsGA	GRCh38
NC_000002.11:g.200213701_200213702delinsGA , CM000664.1:g.200213701_200213702delinsGA	GRCh37
NC_000002.10:g.199921946_199921947delinsGA	NCBI36
NG_016976.1:g.127288_127289delinsTC
NG_016976.2:g.127288_127289delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428695.6:c.541_542delinsTC	ENSP00000388581.1:p.Ser181=
ENST00000700191.1:c.541_542delinsTC	ENSP00000514853.1:p.Ser181=
ENST00000700193.1:c.895_896delinsTC	ENSP00000514854.1:p.Ser299=
ENST00000700208.1:c.347-76307_347-76306delinsTC	ENSP00000514860.1:n.347-76307_347-76306delinsTC
ENST00000700210.1:c.549_550delinsTC
ENST00000417098.6:c.895_896delinsTC MANE Select	ENSP00000401112.1:p.Ser299=
ENST00000260926.9:c.895_896delinsTC	ENSP00000260926.5:p.Ser299=
ENST00000417098.5:c.895_896delinsTC	ENSP00000401112.1:p.Ser299=
ENST00000428695.5:c.541_542delinsTC	ENSP00000388581.1:p.Ser181=
ENST00000443023.5:c.718_719delinsTC	ENSP00000388764.1:p.Ser240=
ENST00000457245.5:c.895_896delinsTC	ENSP00000405420.1:p.Ser299=
ENST00000483346.2:n.534_535delinsTC
ENST00000614512.4:c.541_542delinsTC	ENSP00000483287.1:p.Ser181=
NM_001172509.1:c.895_896delinsTC	NP_001165980.1:p.Ser299=
NM_001172517.1:c.895_896delinsTC	NP_001165988.1:p.Ser299=
NM_015265.3:c.895_896delinsTC	NP_056080.1:p.Ser299=
XM_005246396.1:c.721_722delinsTC	XP_005246453.1:p.Ser241=
XM_006712372.1:c.895_896delinsTC	XP_006712435.1:p.Ser299=
XM_011510840.1:c.895_896delinsTC	XP_011509142.1:p.Ser299=
XM_005246396.3:c.721_722delinsTC	XP_005246453.1:p.Ser241=
XM_011510840.3:c.895_896delinsTC	XP_011509142.1:p.Ser299=
XM_017003656.1:c.721_722delinsTC	XP_016859145.1:p.Ser241=
XM_024452767.1:c.472_473delinsTC	XP_024308535.1:p.Ser158=
XM_024452768.1:c.472_473delinsTC	XP_024308536.1:p.Ser158=
NM_001172509.2:c.895_896delinsTC MANE Select	NP_001165980.1:p.Ser299=
NM_015265.4:c.895_896delinsTC	NP_056080.1:p.Ser299=