Canonical Allele Identifier: CA2573133426

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1686309
• ClinVar RCV Id: RCV002246822
• dbSNP Id: rs2149872634

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389887_144389888insTC , CM000664.2:g.144389887_144389888insTC	GRCh38
NC_000002.11:g.145147454_145147455insTC , CM000664.1:g.145147454_145147455insTC	GRCh37
NC_000002.10:g.144863924_144863925insTC	NCBI36
NG_016431.1:g.135504_135505insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3057_*3058insGA	ENSP00000508434.1:n.*3057_*3058insGA
ENST00000440875.6:c.2431_2432insGA	ENSP00000475553.3:p.Tyr811Ter
ENST00000627532.3:c.3208_3209insGA MANE Select	ENSP00000487174.1:p.Tyr1070Ter
ENST00000636026.2:c.3208_3209insGA	ENSP00000490776.1:p.Tyr1070Ter
ENST00000636179.1:n.3177_3178insGA
ENST00000636413.1:c.2872_2873insGA	ENSP00000490508.1:p.Tyr958Ter
ENST00000636471.1:c.3283_3284insGA	ENSP00000490317.1:p.Tyr1095Ter
ENST00000636732.2:c.*2925_*2926insGA	ENSP00000490175.1:n.*2925_*2926insGA
ENST00000636820.1:n.3308_3309insGA
ENST00000637045.1:c.2872_2873insGA	ENSP00000490141.1:p.Tyr958Ter
ENST00000637304.1:c.2872_2873insGA	ENSP00000490872.1:p.Tyr958Ter
ENST00000638007.1:c.2872_2873insGA	ENSP00000490723.1:p.Tyr958Ter
ENST00000638087.1:c.2872_2873insGA	ENSP00000490673.1:p.Tyr958Ter
ENST00000638128.1:c.2431_2432insGA	ENSP00000490934.1:p.Tyr811Ter
ENST00000639389.1:c.151+6524_151+6525insGA	ENSP00000492572.1:n.151+6524_151+6525insGA
ENST00000647488.1:c.428_429insGA	ENSP00000494820.1:n.428_429insGA
ENST00000675069.1:c.739_740insGA	ENSP00000502467.1:p.Tyr247Ter
ENST00000303660.8:c.3205_3206insGA	ENSP00000302501.4:p.Tyr1069Ter
ENST00000409487.7:c.3208_3209insGA	ENSP00000386854.2:p.Tyr1070Ter
ENST00000419938.5:c.656-1006_656-1005insGA	ENSP00000394777.2:n.656-1006_656-1005insGA
ENST00000539609.7:c.3136_3137insGA	ENSP00000443792.2:p.Tyr1046Ter
ENST00000558170.6:c.3208_3209insGA	ENSP00000454157.1:p.Tyr1070Ter
ENST00000627532.2:c.3208_3209insGA	ENSP00000487174.1:p.Tyr1070Ter
NM_001171653.1:c.3136_3137insGA	NP_001165124.1:p.Tyr1046Ter
NM_014795.3:c.3208_3209insGA	NP_055610.1:p.Tyr1070Ter
XM_006712881.2:c.3208_3209insGA	XP_006712944.1:p.Tyr1070Ter
XM_006712882.2:c.3208_3209insGA	XP_006712945.1:p.Tyr1070Ter
XM_011512231.1:c.3199_3200insGA	XP_011510533.1:p.Tyr1067Ter
XM_011512232.1:c.3187_3188insGA	XP_011510534.1:p.Tyr1063Ter
NM_014795.4:c.3208_3209insGA MANE Select	NP_055610.1:p.Tyr1070Ter
NM_001171653.2:c.3136_3137insGA	NP_001165124.1:p.Tyr1046Ter