Canonical Allele Identifier: CA348701210

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147542G>C (hg19) ; chr2:g.144389975G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389975G>C , CM000664.2:g.144389975G>C	GRCh38
NC_000002.11:g.145147542G>C , CM000664.1:g.145147542G>C	GRCh37
NC_000002.10:g.144864012G>C	NCBI36
NG_016431.1:g.135417C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2970C>G	ENSP00000508434.1:n.*2970C>G
ENST00000440875.6:c.2344C>G	ENSP00000475553.3:p.His782Asp
ENST00000627532.3:c.3121C>G MANE Select	ENSP00000487174.1:p.His1041Asp
ENST00000636026.2:c.3121C>G	ENSP00000490776.1:p.His1041Asp
ENST00000636179.1:n.3090C>G
ENST00000636413.1:c.2785C>G	ENSP00000490508.1:p.His929Asp
ENST00000636471.1:c.3196C>G	ENSP00000490317.1:p.His1066Asp
ENST00000636732.2:c.*2838C>G	ENSP00000490175.1:n.*2838C>G
ENST00000636820.1:n.3221C>G
ENST00000637045.1:c.2785C>G	ENSP00000490141.1:p.His929Asp
ENST00000637304.1:c.2785C>G	ENSP00000490872.1:p.His929Asp
ENST00000638007.1:c.2785C>G	ENSP00000490723.1:p.His929Asp
ENST00000638087.1:c.2785C>G	ENSP00000490673.1:p.His929Asp
ENST00000638128.1:c.2344C>G	ENSP00000490934.1:p.His782Asp
ENST00000639389.1:c.151+6437C>G	ENSP00000492572.1:n.151+6437C>G
ENST00000647488.1:c.341C>G	ENSP00000494820.1:n.341C>G
ENST00000675069.1:c.652C>G	ENSP00000502467.1:p.His218Asp
ENST00000303660.8:c.3118C>G	ENSP00000302501.4:p.His1040Asp
ENST00000409487.7:c.3121C>G	ENSP00000386854.2:p.His1041Asp
ENST00000419938.5:c.656-1093C>G	ENSP00000394777.2:n.656-1093C>G
ENST00000539609.7:c.3049C>G	ENSP00000443792.2:p.His1017Asp
ENST00000558170.6:c.3121C>G	ENSP00000454157.1:p.His1041Asp
ENST00000627532.2:c.3121C>G	ENSP00000487174.1:p.His1041Asp
NM_001171653.1:c.3049C>G	NP_001165124.1:p.His1017Asp
NM_014795.3:c.3121C>G	NP_055610.1:p.His1041Asp
XM_006712881.2:c.3121C>G	XP_006712944.1:p.His1041Asp
XM_006712882.2:c.3121C>G	XP_006712945.1:p.His1041Asp
XM_011512231.1:c.3112C>G	XP_011510533.1:p.His1038Asp
XM_011512232.1:c.3100C>G	XP_011510534.1:p.His1034Asp
NM_014795.4:c.3121C>G MANE Select	NP_055610.1:p.His1041Asp
NM_001171653.2:c.3049C>G	NP_001165124.1:p.His1017Asp