Canonical Allele Identifier: CA348699197

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147179C>A (hg19) ; chr2:g.144389612C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389612C>A , CM000664.2:g.144389612C>A	GRCh38
NC_000002.11:g.145147179C>A , CM000664.1:g.145147179C>A	GRCh37
NC_000002.10:g.144863649C>A	NCBI36
NG_016431.1:g.135780G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3333G>T	ENSP00000508434.1:n.*3333G>T
ENST00000440875.6:c.2707G>T	ENSP00000475553.3:p.Glu903Ter
ENST00000627532.3:c.3484G>T MANE Select	ENSP00000487174.1:p.Glu1162Ter
ENST00000636026.2:c.3372G>T	ENSP00000490776.1:p.Arg1124Ser
ENST00000636179.1:n.3453G>T
ENST00000636413.1:c.3148G>T	ENSP00000490508.1:p.Glu1050Ter
ENST00000636471.1:c.3559G>T	ENSP00000490317.1:p.Glu1187Ter
ENST00000636732.2:c.*3201G>T	ENSP00000490175.1:n.*3201G>T
ENST00000636820.1:n.3584G>T
ENST00000637045.1:c.3148G>T	ENSP00000490141.1:p.Glu1050Ter
ENST00000637304.1:c.3148G>T	ENSP00000490872.1:p.Glu1050Ter
ENST00000638007.1:c.3148G>T	ENSP00000490723.1:p.Glu1050Ter
ENST00000638087.1:c.3148G>T	ENSP00000490673.1:p.Glu1050Ter
ENST00000638128.1:c.2707G>T	ENSP00000490934.1:p.Glu903Ter
ENST00000639389.1:c.151+6800G>T	ENSP00000492572.1:n.151+6800G>T
ENST00000647488.1:c.704G>T	ENSP00000494820.1:n.704G>T
ENST00000675069.1:c.1015G>T	ENSP00000502467.1:p.Glu339Ter
ENST00000303660.8:c.3481G>T	ENSP00000302501.4:p.Glu1161Ter
ENST00000409487.7:c.3484G>T	ENSP00000386854.2:p.Glu1162Ter
ENST00000419938.5:c.656-730G>T	ENSP00000394777.2:n.656-730G>T
ENST00000539609.7:c.3412G>T	ENSP00000443792.2:p.Glu1138Ter
ENST00000558170.6:c.3484G>T	ENSP00000454157.1:p.Glu1162Ter
ENST00000627532.2:c.3484G>T	ENSP00000487174.1:p.Glu1162Ter
NM_001171653.1:c.3412G>T	NP_001165124.1:p.Glu1138Ter
NM_014795.3:c.3484G>T	NP_055610.1:p.Glu1162Ter
XM_006712881.2:c.3484G>T	XP_006712944.1:p.Glu1162Ter
XM_006712882.2:c.3484G>T	XP_006712945.1:p.Glu1162Ter
XM_011512231.1:c.3475G>T	XP_011510533.1:p.Glu1159Ter
XM_011512232.1:c.3463G>T	XP_011510534.1:p.Glu1155Ter
NM_014795.4:c.3484G>T MANE Select	NP_055610.1:p.Glu1162Ter
NM_001171653.2:c.3412G>T	NP_001165124.1:p.Glu1138Ter