Canonical Allele Identifier: CA223159

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 95634
• ClinVar RCV Id: RCV000081668
• dbSNP Id: rs398124279
• MyVariant Identifiers: chr2:g.145147584_145147586del (hg19) ; chr2:g.145147584_145147586delGTG (hg19) ; chr2:g.144390017_144390019del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144390019_144390021del , CM000664.2:g.144390019_144390021del	GRCh38
NC_000002.11:g.145147586_145147588del , CM000664.1:g.145147586_145147588del	GRCh37
NC_000002.10:g.144864056_144864058del	NCBI36
NG_016431.1:g.135373_135375del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2926_*2928del	ENSP00000508434.1:n.*2926_*2928del
ENST00000440875.6:c.2300_2302del	ENSP00000475553.3:p.Pro767del
ENST00000627532.3:c.3077_3079del MANE Select	ENSP00000487174.1:p.Pro1026del
ENST00000636026.2:c.3077_3079del	ENSP00000490776.1:p.Pro1026del
ENST00000636179.1:n.3046_3048del
ENST00000636413.1:c.2741_2743del	ENSP00000490508.1:p.Pro914del
ENST00000636471.1:c.3152_3154del	ENSP00000490317.1:p.Pro1051del
ENST00000636732.2:c.*2794_*2796del	ENSP00000490175.1:n.*2794_*2796del
ENST00000636820.1:n.3177_3179del
ENST00000637045.1:c.2741_2743del	ENSP00000490141.1:p.Pro914del
ENST00000637304.1:c.2741_2743del	ENSP00000490872.1:p.Pro914del
ENST00000638007.1:c.2741_2743del	ENSP00000490723.1:p.Pro914del
ENST00000638087.1:c.2741_2743del	ENSP00000490673.1:p.Pro914del
ENST00000638128.1:c.2300_2302del	ENSP00000490934.1:p.Pro767del
ENST00000639389.1:c.151+6393_151+6395del	ENSP00000492572.1:n.151+6393_151+6395del
ENST00000647488.1:c.297_299del	ENSP00000494820.1:n.297_299del
ENST00000675069.1:c.608_610del	ENSP00000502467.1:p.Pro203del
ENST00000303660.8:c.3074_3076del	ENSP00000302501.4:p.Pro1025del
ENST00000409487.7:c.3077_3079del	ENSP00000386854.2:p.Pro1026del
ENST00000419938.5:c.656-1137_656-1135del	ENSP00000394777.2:n.656-1137_656-1135del
ENST00000539609.7:c.3005_3007del	ENSP00000443792.2:p.Pro1002del
ENST00000558170.6:c.3077_3079del	ENSP00000454157.1:p.Pro1026del
ENST00000627532.2:c.3077_3079del	ENSP00000487174.1:p.Pro1026del
NM_001171653.1:c.3005_3007del	NP_001165124.1:p.Pro1002del
NM_014795.3:c.3077_3079del	NP_055610.1:p.Pro1026del
XM_006712881.2:c.3077_3079del	XP_006712944.1:p.Pro1026del
XM_006712882.2:c.3077_3079del	XP_006712945.1:p.Pro1026del
XM_011512231.1:c.3068_3070del	XP_011510533.1:p.Pro1023del
XM_011512232.1:c.3056_3058del	XP_011510534.1:p.Pro1019del
NM_014795.4:c.3077_3079del MANE Select	NP_055610.1:p.Pro1026del
NM_001171653.2:c.3005_3007del	NP_001165124.1:p.Pro1002del