Canonical Allele Identifier: CA348699786

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147365G>C (hg19) ; chr2:g.144389798G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389798G>C , CM000664.2:g.144389798G>C	GRCh38
NC_000002.11:g.145147365G>C , CM000664.1:g.145147365G>C	GRCh37
NC_000002.10:g.144863835G>C	NCBI36
NG_016431.1:g.135594C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3147C>G	ENSP00000508434.1:n.*3147C>G
ENST00000440875.6:c.2521C>G	ENSP00000475553.3:p.His841Asp
ENST00000627532.3:c.3298C>G MANE Select	ENSP00000487174.1:p.His1100Asp
ENST00000636026.2:c.3231-45C>G	ENSP00000490776.1:n.3231-45C>G
ENST00000636179.1:n.3267C>G
ENST00000636413.1:c.2962C>G	ENSP00000490508.1:p.His988Asp
ENST00000636471.1:c.3373C>G	ENSP00000490317.1:p.His1125Asp
ENST00000636732.2:c.*3015C>G	ENSP00000490175.1:n.*3015C>G
ENST00000636820.1:n.3398C>G
ENST00000637045.1:c.2962C>G	ENSP00000490141.1:p.His988Asp
ENST00000637304.1:c.2962C>G	ENSP00000490872.1:p.His988Asp
ENST00000638007.1:c.2962C>G	ENSP00000490723.1:p.His988Asp
ENST00000638087.1:c.2962C>G	ENSP00000490673.1:p.His988Asp
ENST00000638128.1:c.2521C>G	ENSP00000490934.1:p.His841Asp
ENST00000639389.1:c.151+6614C>G	ENSP00000492572.1:n.151+6614C>G
ENST00000647488.1:c.518C>G	ENSP00000494820.1:n.518C>G
ENST00000675069.1:c.829C>G	ENSP00000502467.1:p.His277Asp
ENST00000303660.8:c.3295C>G	ENSP00000302501.4:p.His1099Asp
ENST00000409487.7:c.3298C>G	ENSP00000386854.2:p.His1100Asp
ENST00000419938.5:c.656-916C>G	ENSP00000394777.2:n.656-916C>G
ENST00000539609.7:c.3226C>G	ENSP00000443792.2:p.His1076Asp
ENST00000558170.6:c.3298C>G	ENSP00000454157.1:p.His1100Asp
ENST00000627532.2:c.3298C>G	ENSP00000487174.1:p.His1100Asp
NM_001171653.1:c.3226C>G	NP_001165124.1:p.His1076Asp
NM_014795.3:c.3298C>G	NP_055610.1:p.His1100Asp
XM_006712881.2:c.3298C>G	XP_006712944.1:p.His1100Asp
XM_006712882.2:c.3298C>G	XP_006712945.1:p.His1100Asp
XM_011512231.1:c.3289C>G	XP_011510533.1:p.His1097Asp
XM_011512232.1:c.3277C>G	XP_011510534.1:p.His1093Asp
NM_014795.4:c.3298C>G MANE Select	NP_055610.1:p.His1100Asp
NM_001171653.2:c.3226C>G	NP_001165124.1:p.His1076Asp