Canonical Allele Identifier: CA429445193

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144399264-A-G
• MyVariant Identifiers: chr2:g.145156831A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399264A>G , CM000664.2:g.144399264A>G	GRCh38
NC_000002.11:g.145156831A>G , CM000664.1:g.145156831A>G	GRCh37
NC_000002.10:g.144873301A>G	NCBI36
NG_016431.1:g.126128T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1772T>C	ENSP00000508434.1:n.*1772T>C
ENST00000440875.6:c.1146T>C	ENSP00000475553.3:p.Ser382=
ENST00000627532.3:c.1923T>C MANE Select	ENSP00000487174.1:p.Ser641=
ENST00000636026.2:c.1923T>C	ENSP00000490776.1:p.Ser641=
ENST00000636179.1:n.1892T>C
ENST00000636413.1:c.1587T>C	ENSP00000490508.1:p.Ser529=
ENST00000636471.1:c.1998T>C	ENSP00000490317.1:p.Ser666=
ENST00000636732.2:c.*1640T>C	ENSP00000490175.1:n.*1640T>C
ENST00000636820.1:n.2023T>C
ENST00000637045.1:c.1587T>C	ENSP00000490141.1:p.Ser529=
ENST00000637304.1:c.1587T>C	ENSP00000490872.1:p.Ser529=
ENST00000638007.1:c.1587T>C	ENSP00000490723.1:p.Ser529=
ENST00000638087.1:c.1587T>C	ENSP00000490673.1:p.Ser529=
ENST00000638128.1:c.1146T>C	ENSP00000490934.1:p.Ser382=
ENST00000675069.1:c.-133-414T>C	ENSP00000502467.1:n.-133-414T>C
ENST00000675145.1:n.2471T>C
ENST00000303660.8:c.1920T>C	ENSP00000302501.4:p.Ser640=
ENST00000409487.7:c.1923T>C	ENSP00000386854.2:p.Ser641=
ENST00000419938.5:c.655+1935T>C	ENSP00000394777.2:n.655+1935T>C
ENST00000427902.5:c.2010T>C	ENSP00000395496.2:p.Ser670=
ENST00000440875.5:c.1167+273T>C	ENSP00000475553.2:n.1167+273T>C
ENST00000539609.7:c.1851T>C	ENSP00000443792.2:p.Ser617=
ENST00000558170.6:c.1923T>C	ENSP00000454157.1:p.Ser641=
ENST00000627532.2:c.1923T>C	ENSP00000487174.1:p.Ser641=
NM_001171653.1:c.1851T>C	NP_001165124.1:p.Ser617=
NM_014795.3:c.1923T>C	NP_055610.1:p.Ser641=
XM_006712881.2:c.1923T>C	XP_006712944.1:p.Ser641=
XM_006712882.2:c.1923T>C	XP_006712945.1:p.Ser641=
XM_011512231.1:c.1914T>C	XP_011510533.1:p.Ser638=
XM_011512232.1:c.1902T>C	XP_011510534.1:p.Ser634=
NM_014795.4:c.1923T>C MANE Select	NP_055610.1:p.Ser641=
NM_001171653.2:c.1851T>C	NP_001165124.1:p.Ser617=