Canonical Allele Identifier: CA348698572

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147033C>T (hg19) ; chr2:g.144389466C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389466C>T , CM000664.2:g.144389466C>T	GRCh38
NC_000002.11:g.145147033C>T , CM000664.1:g.145147033C>T	GRCh37
NC_000002.10:g.144863503C>T	NCBI36
NG_016431.1:g.135926G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3479G>A	ENSP00000508434.1:n.*3479G>A
ENST00000440875.6:c.2853G>A	ENSP00000475553.3:p.Met951Ile
ENST00000627532.3:c.3630G>A MANE Select	ENSP00000487174.1:p.Met1210Ile
ENST00000636026.2:c.3518G>A	ENSP00000490776.1:p.Trp1173Ter
ENST00000636179.1:n.3599G>A
ENST00000636413.1:c.3294G>A	ENSP00000490508.1:p.Met1098Ile
ENST00000636471.1:c.3705G>A	ENSP00000490317.1:p.Met1235Ile
ENST00000636732.2:c.*3347G>A	ENSP00000490175.1:n.*3347G>A
ENST00000636820.1:n.3730G>A
ENST00000637045.1:c.3294G>A	ENSP00000490141.1:p.Met1098Ile
ENST00000637304.1:c.3294G>A	ENSP00000490872.1:p.Met1098Ile
ENST00000638007.1:c.3294G>A	ENSP00000490723.1:p.Met1098Ile
ENST00000638087.1:c.3294G>A	ENSP00000490673.1:p.Met1098Ile
ENST00000638128.1:c.2853G>A	ENSP00000490934.1:p.Met951Ile
ENST00000639389.1:c.151+6946G>A	ENSP00000492572.1:n.151+6946G>A
ENST00000647488.1:c.850G>A	ENSP00000494820.1:n.850G>A
ENST00000675069.1:c.1161G>A	ENSP00000502467.1:p.Met387Ile
ENST00000303660.8:c.3627G>A	ENSP00000302501.4:p.Met1209Ile
ENST00000409487.7:c.3630G>A	ENSP00000386854.2:p.Met1210Ile
ENST00000419938.5:c.656-584G>A	ENSP00000394777.2:n.656-584G>A
ENST00000539609.7:c.3558G>A	ENSP00000443792.2:p.Met1186Ile
ENST00000558170.6:c.3630G>A	ENSP00000454157.1:p.Met1210Ile
ENST00000627532.2:c.3630G>A	ENSP00000487174.1:p.Met1210Ile
NM_001171653.1:c.3558G>A	NP_001165124.1:p.Met1186Ile
NM_014795.3:c.3630G>A	NP_055610.1:p.Met1210Ile
XM_006712881.2:c.3630G>A	XP_006712944.1:p.Met1210Ile
XM_006712882.2:c.3630G>A	XP_006712945.1:p.Met1210Ile
XM_011512231.1:c.3621G>A	XP_011510533.1:p.Met1207Ile
XM_011512232.1:c.3609G>A	XP_011510534.1:p.Met1203Ile
NM_014795.4:c.3630G>A MANE Select	NP_055610.1:p.Met1210Ile
NM_001171653.2:c.3558G>A	NP_001165124.1:p.Met1186Ile