Canonical Allele Identifier: CA348699793

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147367C>G (hg19) ; chr2:g.144389800C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389800C>G , CM000664.2:g.144389800C>G	GRCh38
NC_000002.11:g.145147367C>G , CM000664.1:g.145147367C>G	GRCh37
NC_000002.10:g.144863837C>G	NCBI36
NG_016431.1:g.135592G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3145G>C	ENSP00000508434.1:n.*3145G>C
ENST00000440875.6:c.2519G>C	ENSP00000475553.3:p.Gly840Ala
ENST00000627532.3:c.3296G>C MANE Select	ENSP00000487174.1:p.Gly1099Ala
ENST00000636026.2:c.3231-47G>C	ENSP00000490776.1:n.3231-47G>C
ENST00000636179.1:n.3265G>C
ENST00000636413.1:c.2960G>C	ENSP00000490508.1:p.Gly987Ala
ENST00000636471.1:c.3371G>C	ENSP00000490317.1:p.Gly1124Ala
ENST00000636732.2:c.*3013G>C	ENSP00000490175.1:n.*3013G>C
ENST00000636820.1:n.3396G>C
ENST00000637045.1:c.2960G>C	ENSP00000490141.1:p.Gly987Ala
ENST00000637304.1:c.2960G>C	ENSP00000490872.1:p.Gly987Ala
ENST00000638007.1:c.2960G>C	ENSP00000490723.1:p.Gly987Ala
ENST00000638087.1:c.2960G>C	ENSP00000490673.1:p.Gly987Ala
ENST00000638128.1:c.2519G>C	ENSP00000490934.1:p.Gly840Ala
ENST00000639389.1:c.151+6612G>C	ENSP00000492572.1:n.151+6612G>C
ENST00000647488.1:c.516G>C	ENSP00000494820.1:n.516G>C
ENST00000675069.1:c.827G>C	ENSP00000502467.1:p.Gly276Ala
ENST00000303660.8:c.3293G>C	ENSP00000302501.4:p.Gly1098Ala
ENST00000409487.7:c.3296G>C	ENSP00000386854.2:p.Gly1099Ala
ENST00000419938.5:c.656-918G>C	ENSP00000394777.2:n.656-918G>C
ENST00000539609.7:c.3224G>C	ENSP00000443792.2:p.Gly1075Ala
ENST00000558170.6:c.3296G>C	ENSP00000454157.1:p.Gly1099Ala
ENST00000627532.2:c.3296G>C	ENSP00000487174.1:p.Gly1099Ala
NM_001171653.1:c.3224G>C	NP_001165124.1:p.Gly1075Ala
NM_014795.3:c.3296G>C	NP_055610.1:p.Gly1099Ala
XM_006712881.2:c.3296G>C	XP_006712944.1:p.Gly1099Ala
XM_006712882.2:c.3296G>C	XP_006712945.1:p.Gly1099Ala
XM_011512231.1:c.3287G>C	XP_011510533.1:p.Gly1096Ala
XM_011512232.1:c.3275G>C	XP_011510534.1:p.Gly1092Ala
NM_014795.4:c.3296G>C MANE Select	NP_055610.1:p.Gly1099Ala
NM_001171653.2:c.3224G>C	NP_001165124.1:p.Gly1075Ala