Canonical Allele Identifier: CA284669

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 56826
• ClinVar RCV Id: RCV000050218 ; RCV002513706
• dbSNP Id: rs397515448
• MyVariant Identifiers: chr2:g.145147452A>G (hg19) ; chr2:g.144389885A>G (hg38)
• PubMed: PMID:23466526

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389885A>G , CM000664.2:g.144389885A>G	GRCh38
NC_000002.11:g.145147452A>G , CM000664.1:g.145147452A>G	GRCh37
NC_000002.10:g.144863922A>G	NCBI36
NG_016431.1:g.135507T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3060T>C	ENSP00000508434.1:n.*3060T>C
ENST00000440875.6:c.2434T>C	ENSP00000475553.3:p.Ser812Pro
ENST00000627532.3:c.3211T>C MANE Select	ENSP00000487174.1:p.Ser1071Pro
ENST00000636026.2:c.3211T>C	ENSP00000490776.1:p.Ser1071Pro
ENST00000636179.1:n.3180T>C
ENST00000636413.1:c.2875T>C	ENSP00000490508.1:p.Ser959Pro
ENST00000636471.1:c.3286T>C	ENSP00000490317.1:p.Ser1096Pro
ENST00000636732.2:c.*2928T>C	ENSP00000490175.1:n.*2928T>C
ENST00000636820.1:n.3311T>C
ENST00000637045.1:c.2875T>C	ENSP00000490141.1:p.Ser959Pro
ENST00000637304.1:c.2875T>C	ENSP00000490872.1:p.Ser959Pro
ENST00000638007.1:c.2875T>C	ENSP00000490723.1:p.Ser959Pro
ENST00000638087.1:c.2875T>C	ENSP00000490673.1:p.Ser959Pro
ENST00000638128.1:c.2434T>C	ENSP00000490934.1:p.Ser812Pro
ENST00000639389.1:c.151+6527T>C	ENSP00000492572.1:n.151+6527T>C
ENST00000647488.1:c.431T>C	ENSP00000494820.1:n.431T>C
ENST00000675069.1:c.742T>C	ENSP00000502467.1:p.Ser248Pro
ENST00000303660.8:c.3208T>C	ENSP00000302501.4:p.Ser1070Pro
ENST00000409487.7:c.3211T>C	ENSP00000386854.2:p.Ser1071Pro
ENST00000419938.5:c.656-1003T>C	ENSP00000394777.2:n.656-1003T>C
ENST00000539609.7:c.3139T>C	ENSP00000443792.2:p.Ser1047Pro
ENST00000558170.6:c.3211T>C	ENSP00000454157.1:p.Ser1071Pro
ENST00000627532.2:c.3211T>C	ENSP00000487174.1:p.Ser1071Pro
NM_001171653.1:c.3139T>C	NP_001165124.1:p.Ser1047Pro
NM_014795.3:c.3211T>C	NP_055610.1:p.Ser1071Pro
XM_006712881.2:c.3211T>C	XP_006712944.1:p.Ser1071Pro
XM_006712882.2:c.3211T>C	XP_006712945.1:p.Ser1071Pro
XM_011512231.1:c.3202T>C	XP_011510533.1:p.Ser1068Pro
XM_011512232.1:c.3190T>C	XP_011510534.1:p.Ser1064Pro
NM_014795.4:c.3211T>C MANE Select	NP_055610.1:p.Ser1071Pro
NM_001171653.2:c.3139T>C	NP_001165124.1:p.Ser1047Pro