Canonical Allele Identifier: CA350387908

Gene: SATB2

Linked Data

• MyVariant Identifiers: chr2:g.200213705G>C (hg19) ; chr2:g.199348982G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199348982G>C , CM000664.2:g.199348982G>C	GRCh38
NC_000002.11:g.200213705G>C , CM000664.1:g.200213705G>C	GRCh37
NC_000002.10:g.199921950G>C	NCBI36
NG_016976.1:g.127285C>G
NG_016976.2:g.127285C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428695.6:c.538C>G	ENSP00000388581.1:p.Leu180Val
ENST00000700191.1:c.538C>G	ENSP00000514853.1:p.Leu180Val
ENST00000700193.1:c.892C>G	ENSP00000514854.1:p.Leu298Val
ENST00000700208.1:c.347-76310C>G	ENSP00000514860.1:n.347-76310C>G
ENST00000700210.1:c.546C>G
ENST00000417098.6:c.892C>G MANE Select	ENSP00000401112.1:p.Leu298Val
ENST00000260926.9:c.892C>G	ENSP00000260926.5:p.Leu298Val
ENST00000417098.5:c.892C>G	ENSP00000401112.1:p.Leu298Val
ENST00000428695.5:c.538C>G	ENSP00000388581.1:p.Leu180Val
ENST00000443023.5:c.715C>G	ENSP00000388764.1:p.Leu239Val
ENST00000457245.5:c.892C>G	ENSP00000405420.1:p.Leu298Val
ENST00000483346.2:n.531C>G
ENST00000614512.4:c.538C>G	ENSP00000483287.1:p.Leu180Val
NM_001172509.1:c.892C>G	NP_001165980.1:p.Leu298Val
NM_001172517.1:c.892C>G	NP_001165988.1:p.Leu298Val
NM_015265.3:c.892C>G	NP_056080.1:p.Leu298Val
XM_005246396.1:c.718C>G	XP_005246453.1:p.Leu240Val
XM_006712372.1:c.892C>G	XP_006712435.1:p.Leu298Val
XM_011510840.1:c.892C>G	XP_011509142.1:p.Leu298Val
XM_005246396.3:c.718C>G	XP_005246453.1:p.Leu240Val
XM_011510840.3:c.892C>G	XP_011509142.1:p.Leu298Val
XM_017003656.1:c.718C>G	XP_016859145.1:p.Leu240Val
XM_024452767.1:c.469C>G	XP_024308535.1:p.Leu157Val
XM_024452768.1:c.469C>G	XP_024308536.1:p.Leu157Val
NM_001172509.2:c.892C>G MANE Select	NP_001165980.1:p.Leu298Val
NM_015265.4:c.892C>G	NP_056080.1:p.Leu298Val