Canonical Allele Identifier: CA2577152071

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389733_144389734insCAT , CM000664.2:g.144389733_144389734insCAT	GRCh38
NC_000002.11:g.145147300_145147301insCAT , CM000664.1:g.145147300_145147301insCAT	GRCh37
NC_000002.10:g.144863770_144863771insCAT	NCBI36
NG_016431.1:g.135658_135659insATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3211_*3212insATG	ENSP00000508434.1:n.*3211_*3212insATG
ENST00000440875.6:c.2585_2586insATG	ENSP00000475553.3:p.Tyr862Ter
ENST00000627532.3:c.3362_3363insATG MANE Select	ENSP00000487174.1:p.Tyr1121Ter
ENST00000636026.2:c.3250_3251insATG	ENSP00000490776.1:p.Thr1084delinsAsnAla
ENST00000636179.1:n.3331_3332insATG
ENST00000636413.1:c.3026_3027insATG	ENSP00000490508.1:p.Tyr1009Ter
ENST00000636471.1:c.3437_3438insATG	ENSP00000490317.1:p.Tyr1146Ter
ENST00000636732.2:c.*3079_*3080insATG	ENSP00000490175.1:n.*3079_*3080insATG
ENST00000636820.1:n.3462_3463insATG
ENST00000637045.1:c.3026_3027insATG	ENSP00000490141.1:p.Tyr1009Ter
ENST00000637304.1:c.3026_3027insATG	ENSP00000490872.1:p.Tyr1009Ter
ENST00000638007.1:c.3026_3027insATG	ENSP00000490723.1:p.Tyr1009Ter
ENST00000638087.1:c.3026_3027insATG	ENSP00000490673.1:p.Tyr1009Ter
ENST00000638128.1:c.2585_2586insATG	ENSP00000490934.1:p.Tyr862Ter
ENST00000639389.1:c.151+6678_151+6679insATG	ENSP00000492572.1:n.151+6678_151+6679insA...
ENST00000647488.1:c.582_583insATG	ENSP00000494820.1:n.582_583insATG
ENST00000675069.1:c.893_894insATG	ENSP00000502467.1:p.Tyr298Ter
ENST00000303660.8:c.3359_3360insATG	ENSP00000302501.4:p.Tyr1120Ter
ENST00000409487.7:c.3362_3363insATG	ENSP00000386854.2:p.Tyr1121Ter
ENST00000419938.5:c.656-852_656-851insATG	ENSP00000394777.2:n.656-852_656-851insATG...
ENST00000539609.7:c.3290_3291insATG	ENSP00000443792.2:p.Tyr1097Ter
ENST00000558170.6:c.3362_3363insATG	ENSP00000454157.1:p.Tyr1121Ter
ENST00000627532.2:c.3362_3363insATG	ENSP00000487174.1:p.Tyr1121Ter
NM_001171653.1:c.3290_3291insATG	NP_001165124.1:p.Tyr1097Ter
NM_014795.3:c.3362_3363insATG	NP_055610.1:p.Tyr1121Ter
XM_006712881.2:c.3362_3363insATG	XP_006712944.1:p.Tyr1121Ter
XM_006712882.2:c.3362_3363insATG	XP_006712945.1:p.Tyr1121Ter
XM_011512231.1:c.3353_3354insATG	XP_011510533.1:p.Tyr1118Ter
XM_011512232.1:c.3341_3342insATG	XP_011510534.1:p.Tyr1114Ter
NM_014795.4:c.3362_3363insATG MANE Select	NP_055610.1:p.Tyr1121Ter
NM_001171653.2:c.3290_3291insATG	NP_001165124.1:p.Tyr1097Ter