Canonical Allele Identifier: CA1294884853

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398340C= , CM000664.2:g.144398340C=	GRCh38
NC_000002.11:g.145155907C= , CM000664.1:g.145155907C=	GRCh37
NC_000002.10:g.144872377C=	NCBI36
NG_016431.1:g.127052G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2696G=	ENSP00000508434.1:n.*2696G=
ENST00000440875.6:c.2070G=	ENSP00000475553.3:p.Met690=
ENST00000627532.3:c.2847G= MANE Select	ENSP00000487174.1:p.Met949=
ENST00000636026.2:c.2847G=	ENSP00000490776.1:p.Met949=
ENST00000636179.1:n.2816G=
ENST00000636413.1:c.2511G=	ENSP00000490508.1:p.Met837=
ENST00000636471.1:c.2922G=	ENSP00000490317.1:p.Met974=
ENST00000636732.2:c.*2564G=	ENSP00000490175.1:n.*2564G=
ENST00000636820.1:n.2947G=
ENST00000637045.1:c.2511G=	ENSP00000490141.1:p.Met837=
ENST00000637304.1:c.2511G=	ENSP00000490872.1:p.Met837=
ENST00000638007.1:c.2511G=	ENSP00000490723.1:p.Met837=
ENST00000638087.1:c.2511G=	ENSP00000490673.1:p.Met837=
ENST00000638128.1:c.2070G=	ENSP00000490934.1:p.Met690=
ENST00000675069.1:c.378G=	ENSP00000502467.1:p.Met126=
ENST00000303660.8:c.2844G=	ENSP00000302501.4:p.Met948=
ENST00000409487.7:c.2847G=	ENSP00000386854.2:p.Met949=
ENST00000419938.5:c.655+2859G=	ENSP00000394777.2:n.655+2859G=
ENST00000440875.5:c.1168-412G=	ENSP00000475553.2:n.1168-412G=
ENST00000539609.7:c.2775G=	ENSP00000443792.2:p.Met925=
ENST00000558170.6:c.2847G=	ENSP00000454157.1:p.Met949=
ENST00000627532.2:c.2847G=	ENSP00000487174.1:p.Met949=
NM_001171653.1:c.2775G=	NP_001165124.1:p.Met925=
NM_014795.3:c.2847G=	NP_055610.1:p.Met949=
XM_006712881.2:c.2847G=	XP_006712944.1:p.Met949=
XM_006712882.2:c.2847G=	XP_006712945.1:p.Met949=
XM_011512231.1:c.2838G=	XP_011510533.1:p.Met946=
XM_011512232.1:c.2826G=	XP_011510534.1:p.Met942=
NM_014795.4:c.2847G= MANE Select	NP_055610.1:p.Met949=
NM_001171653.2:c.2775G=	NP_001165124.1:p.Met925=