Canonical Allele Identifier: CA348700252

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147446G>T (hg19) ; chr2:g.144389879G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389879G>T , CM000664.2:g.144389879G>T	GRCh38
NC_000002.11:g.145147446G>T , CM000664.1:g.145147446G>T	GRCh37
NC_000002.10:g.144863916G>T	NCBI36
NG_016431.1:g.135513C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3066C>A	ENSP00000508434.1:n.*3066C>A
ENST00000440875.6:c.2440C>A	ENSP00000475553.3:p.His814Asn
ENST00000627532.3:c.3217C>A MANE Select	ENSP00000487174.1:p.His1073Asn
ENST00000636026.2:c.3217C>A	ENSP00000490776.1:p.His1073Asn
ENST00000636179.1:n.3186C>A
ENST00000636413.1:c.2881C>A	ENSP00000490508.1:p.His961Asn
ENST00000636471.1:c.3292C>A	ENSP00000490317.1:p.His1098Asn
ENST00000636732.2:c.*2934C>A	ENSP00000490175.1:n.*2934C>A
ENST00000636820.1:n.3317C>A
ENST00000637045.1:c.2881C>A	ENSP00000490141.1:p.His961Asn
ENST00000637304.1:c.2881C>A	ENSP00000490872.1:p.His961Asn
ENST00000638007.1:c.2881C>A	ENSP00000490723.1:p.His961Asn
ENST00000638087.1:c.2881C>A	ENSP00000490673.1:p.His961Asn
ENST00000638128.1:c.2440C>A	ENSP00000490934.1:p.His814Asn
ENST00000639389.1:c.151+6533C>A	ENSP00000492572.1:n.151+6533C>A
ENST00000647488.1:c.437C>A	ENSP00000494820.1:n.437C>A
ENST00000675069.1:c.748C>A	ENSP00000502467.1:p.His250Asn
ENST00000303660.8:c.3214C>A	ENSP00000302501.4:p.His1072Asn
ENST00000409487.7:c.3217C>A	ENSP00000386854.2:p.His1073Asn
ENST00000419938.5:c.656-997C>A	ENSP00000394777.2:n.656-997C>A
ENST00000539609.7:c.3145C>A	ENSP00000443792.2:p.His1049Asn
ENST00000558170.6:c.3217C>A	ENSP00000454157.1:p.His1073Asn
ENST00000627532.2:c.3217C>A	ENSP00000487174.1:p.His1073Asn
NM_001171653.1:c.3145C>A	NP_001165124.1:p.His1049Asn
NM_014795.3:c.3217C>A	NP_055610.1:p.His1073Asn
XM_006712881.2:c.3217C>A	XP_006712944.1:p.His1073Asn
XM_006712882.2:c.3217C>A	XP_006712945.1:p.His1073Asn
XM_011512231.1:c.3208C>A	XP_011510533.1:p.His1070Asn
XM_011512232.1:c.3196C>A	XP_011510534.1:p.His1066Asn
NM_014795.4:c.3217C>A MANE Select	NP_055610.1:p.His1073Asn
NM_001171653.2:c.3145C>A	NP_001165124.1:p.His1049Asn