Canonical Allele Identifier: CA348712168

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145157456T>G (hg19) ; chr2:g.144399889T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399889T>G , CM000664.2:g.144399889T>G	GRCh38
NC_000002.11:g.145157456T>G , CM000664.1:g.145157456T>G	GRCh37
NC_000002.10:g.144873926T>G	NCBI36
NG_016431.1:g.125503A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1147A>C	ENSP00000508434.1:n.*1147A>C
ENST00000440875.6:c.521A>C	ENSP00000475553.3:p.Gln174Pro
ENST00000627532.3:c.1298A>C MANE Select	ENSP00000487174.1:p.Gln433Pro
ENST00000636026.2:c.1298A>C	ENSP00000490776.1:p.Gln433Pro
ENST00000636179.1:n.1267A>C
ENST00000636413.1:c.962A>C	ENSP00000490508.1:p.Gln321Pro
ENST00000636471.1:c.1373A>C	ENSP00000490317.1:p.Gln458Pro
ENST00000636732.2:c.*1015A>C	ENSP00000490175.1:n.*1015A>C
ENST00000636820.1:n.1398A>C
ENST00000637045.1:c.962A>C	ENSP00000490141.1:p.Gln321Pro
ENST00000637267.2:c.1298A>C	ENSP00000490293.2:p.Gln433Pro
ENST00000637304.1:c.962A>C	ENSP00000490872.1:p.Gln321Pro
ENST00000638007.1:c.962A>C	ENSP00000490723.1:p.Gln321Pro
ENST00000638087.1:c.962A>C	ENSP00000490673.1:p.Gln321Pro
ENST00000638128.1:c.521A>C	ENSP00000490934.1:p.Gln174Pro
ENST00000675069.1:c.-133-1039A>C	ENSP00000502467.1:n.-133-1039A>C
ENST00000675145.1:n.1846A>C
ENST00000303660.8:c.1295A>C	ENSP00000302501.4:p.Gln432Pro
ENST00000392861.6:c.1382A>C	ENSP00000376601.3:p.Gln461Pro
ENST00000409487.7:c.1298A>C	ENSP00000386854.2:p.Gln433Pro
ENST00000419938.5:c.655+1310A>C	ENSP00000394777.2:n.655+1310A>C
ENST00000427902.5:c.1385A>C	ENSP00000395496.2:p.Gln462Pro
ENST00000440875.5:c.1153+130A>C	ENSP00000475553.2:n.1153+130A>C
ENST00000539609.7:c.1226A>C	ENSP00000443792.2:p.Gln409Pro
ENST00000558170.6:c.1298A>C	ENSP00000454157.1:p.Gln433Pro
ENST00000627532.2:c.1298A>C	ENSP00000487174.1:p.Gln433Pro
NM_001171653.1:c.1226A>C	NP_001165124.1:p.Gln409Pro
NM_014795.3:c.1298A>C	NP_055610.1:p.Gln433Pro
XM_006712881.2:c.1298A>C	XP_006712944.1:p.Gln433Pro
XM_006712882.2:c.1298A>C	XP_006712945.1:p.Gln433Pro
XM_011512231.1:c.1289A>C	XP_011510533.1:p.Gln430Pro
XM_011512232.1:c.1277A>C	XP_011510534.1:p.Gln426Pro
NM_014795.4:c.1298A>C MANE Select	NP_055610.1:p.Gln433Pro
NM_001171653.2:c.1226A>C	NP_001165124.1:p.Gln409Pro