Canonical Allele Identifier: CA1294881257

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389572_144389573delinsTC , CM000664.2:g.144389572_144389573delinsTC	GRCh38
NC_000002.11:g.145147139_145147140delinsTC , CM000664.1:g.145147139_145147140delinsTC	GRCh37
NC_000002.10:g.144863609_144863610delinsTC	NCBI36
NG_016431.1:g.135819_135820delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3372_*3373delinsGA	ENSP00000508434.1:n.*3372_*3373delinsGA
ENST00000440875.6:c.2746_2747delinsGA	ENSP00000475553.3:p.Asp916=
ENST00000627532.3:c.3523_3524delinsGA MANE Select	ENSP00000487174.1:p.Asp1175=
ENST00000636026.2:c.3411_3412delinsGA	ENSP00000490776.1:p.Arg1137=
ENST00000636179.1:n.3492_3493delinsGA
ENST00000636413.1:c.3187_3188delinsGA	ENSP00000490508.1:p.Asp1063=
ENST00000636471.1:c.3598_3599delinsGA	ENSP00000490317.1:p.Asp1200=
ENST00000636732.2:c.*3240_*3241delinsGA	ENSP00000490175.1:n.*3240_*3241delinsGA
ENST00000636820.1:n.3623_3624delinsGA
ENST00000637045.1:c.3187_3188delinsGA	ENSP00000490141.1:p.Asp1063=
ENST00000637304.1:c.3187_3188delinsGA	ENSP00000490872.1:p.Asp1063=
ENST00000638007.1:c.3187_3188delinsGA	ENSP00000490723.1:p.Asp1063=
ENST00000638087.1:c.3187_3188delinsGA	ENSP00000490673.1:p.Asp1063=
ENST00000638128.1:c.2746_2747delinsGA	ENSP00000490934.1:p.Asp916=
ENST00000639389.1:c.151+6839_151+6840delinsGA	ENSP00000492572.1:n.151+6839_151+6840delinsGA
ENST00000647488.1:c.743_744delinsGA	ENSP00000494820.1:n.743_744delinsGA
ENST00000675069.1:c.1054_1055delinsGA	ENSP00000502467.1:p.Asp352=
ENST00000303660.8:c.3520_3521delinsGA	ENSP00000302501.4:p.Asp1174=
ENST00000409487.7:c.3523_3524delinsGA	ENSP00000386854.2:p.Asp1175=
ENST00000419938.5:c.656-691_656-690delinsGA	ENSP00000394777.2:n.656-691_656-690delinsGA
ENST00000539609.7:c.3451_3452delinsGA	ENSP00000443792.2:p.Asp1151=
ENST00000558170.6:c.3523_3524delinsGA	ENSP00000454157.1:p.Asp1175=
ENST00000627532.2:c.3523_3524delinsGA	ENSP00000487174.1:p.Asp1175=
NM_001171653.1:c.3451_3452delinsGA	NP_001165124.1:p.Asp1151=
NM_014795.3:c.3523_3524delinsGA	NP_055610.1:p.Asp1175=
XM_006712881.2:c.3523_3524delinsGA	XP_006712944.1:p.Asp1175=
XM_006712882.2:c.3523_3524delinsGA	XP_006712945.1:p.Asp1175=
XM_011512231.1:c.3514_3515delinsGA	XP_011510533.1:p.Asp1172=
XM_011512232.1:c.3502_3503delinsGA	XP_011510534.1:p.Asp1168=
NM_014795.4:c.3523_3524delinsGA MANE Select	NP_055610.1:p.Asp1175=
NM_001171653.2:c.3451_3452delinsGA	NP_001165124.1:p.Asp1151=