Canonical Allele Identifier: CA350387763

Gene: SATB2

Linked Data

• ClinVar Variation Id: 2444158
• ClinVar RCV Id: RCV003152956
• MyVariant Identifiers: chr2:g.200213642G>A (hg19) ; chr2:g.199348919G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199348919G>A , CM000664.2:g.199348919G>A	GRCh38
NC_000002.11:g.200213642G>A , CM000664.1:g.200213642G>A	GRCh37
NC_000002.10:g.199921887G>A	NCBI36
NG_016976.1:g.127348C>T
NG_016976.2:g.127348C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000428695.6:c.601C>T	ENSP00000388581.1:p.Gln201Ter
ENST00000700191.1:c.601C>T	ENSP00000514853.1:p.Gln201Ter
ENST00000700193.1:c.955C>T	ENSP00000514854.1:p.Gln319Ter
ENST00000700208.1:c.347-76247C>T	ENSP00000514860.1:n.347-76247C>T
ENST00000700210.1:c.609C>T
ENST00000417098.6:c.955C>T MANE Select	ENSP00000401112.1:p.Gln319Ter
ENST00000260926.9:c.955C>T	ENSP00000260926.5:p.Gln319Ter
ENST00000417098.5:c.955C>T	ENSP00000401112.1:p.Gln319Ter
ENST00000428695.5:c.601C>T	ENSP00000388581.1:p.Gln201Ter
ENST00000443023.5:c.778C>T	ENSP00000388764.1:p.Gln260Ter
ENST00000457245.5:c.955C>T	ENSP00000405420.1:p.Gln319Ter
ENST00000483346.2:n.594C>T
ENST00000614512.4:c.601C>T	ENSP00000483287.1:p.Gln201Ter
NM_001172509.1:c.955C>T	NP_001165980.1:p.Gln319Ter
NM_001172517.1:c.955C>T	NP_001165988.1:p.Gln319Ter
NM_015265.3:c.955C>T	NP_056080.1:p.Gln319Ter
XM_005246396.1:c.781C>T	XP_005246453.1:p.Gln261Ter
XM_006712372.1:c.955C>T	XP_006712435.1:p.Gln319Ter
XM_011510840.1:c.955C>T	XP_011509142.1:p.Gln319Ter
XM_005246396.3:c.781C>T	XP_005246453.1:p.Gln261Ter
XM_011510840.3:c.955C>T	XP_011509142.1:p.Gln319Ter
XM_017003656.1:c.781C>T	XP_016859145.1:p.Gln261Ter
XM_024452767.1:c.532C>T	XP_024308535.1:p.Gln178Ter
XM_024452768.1:c.532C>T	XP_024308536.1:p.Gln178Ter
NM_001172509.2:c.955C>T MANE Select	NP_001165980.1:p.Gln319Ter
NM_015265.4:c.955C>T	NP_056080.1:p.Gln319Ter