Canonical Allele Identifier: CA1898130

Gene: ZEB2

Linked Data

• dbSNP Id: rs755868071
• ExAC: 2:145147371 T / TCTCGCGCGC
• gnomAD v2: 2-145147371-T-TCTCGCGCGC
• MyVariant Identifiers: chr2:g.145147371_145147372insCTCGCGCGC (hg19) ; chr2:g.144389804_144389805insCTCGCGCGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389812_144389820dup , CM000664.2:g.144389812_144389820dup	GRCh38
NC_000002.11:g.145147379_145147387dup , CM000664.1:g.145147379_145147387dup	GRCh37
NC_000002.10:g.144863849_144863857dup	NCBI36
NG_016431.1:g.135579_135587dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3132_*3140dup	ENSP00000508434.1:n.*3132_*3140dup
ENST00000440875.6:c.2506_2514dup	ENSP00000475553.3:p.Glu838_Lys839insAlaArgGlu
ENST00000627532.3:c.3283_3291dup MANE Select	ENSP00000487174.1:p.Glu1097_Lys1098insAlaArgGlu
ENST00000636026.2:c.3230+53_3231-52dup	ENSP00000490776.1:n.3230+53_3231-52dup
ENST00000636179.1:n.3252_3260dup
ENST00000636413.1:c.2947_2955dup	ENSP00000490508.1:p.Glu985_Lys986insAlaArgGlu
ENST00000636471.1:c.3358_3366dup	ENSP00000490317.1:p.Glu1122_Lys1123insAlaArgGlu
ENST00000636732.2:c.*3000_*3008dup	ENSP00000490175.1:n.*3000_*3008dup
ENST00000636820.1:n.3383_3391dup
ENST00000637045.1:c.2947_2955dup	ENSP00000490141.1:p.Glu985_Lys986insAlaArgGlu
ENST00000637304.1:c.2947_2955dup	ENSP00000490872.1:p.Glu985_Lys986insAlaArgGlu
ENST00000638007.1:c.2947_2955dup	ENSP00000490723.1:p.Glu985_Lys986insAlaArgGlu
ENST00000638087.1:c.2947_2955dup	ENSP00000490673.1:p.Glu985_Lys986insAlaArgGlu
ENST00000638128.1:c.2506_2514dup	ENSP00000490934.1:p.Glu838_Lys839insAlaArgGlu
ENST00000639389.1:c.151+6599_151+6607dup	ENSP00000492572.1:n.151+6599_151+6607dup
ENST00000647488.1:c.503_511dup	ENSP00000494820.1:n.503_511dup
ENST00000675069.1:c.814_822dup	ENSP00000502467.1:p.Glu274_Lys275insAlaArgGlu
ENST00000303660.8:c.3280_3288dup	ENSP00000302501.4:p.Glu1096_Lys1097insAlaArgGlu
ENST00000409487.7:c.3283_3291dup	ENSP00000386854.2:p.Glu1097_Lys1098insAlaArgGlu
ENST00000419938.5:c.656-931_656-923dup	ENSP00000394777.2:n.656-931_656-923dup
ENST00000539609.7:c.3211_3219dup	ENSP00000443792.2:p.Glu1073_Lys1074insAlaArgGlu
ENST00000558170.6:c.3283_3291dup	ENSP00000454157.1:p.Glu1097_Lys1098insAlaArgGlu
ENST00000627532.2:c.3283_3291dup	ENSP00000487174.1:p.Glu1097_Lys1098insAlaArgGlu
NM_001171653.1:c.3211_3219dup	NP_001165124.1:p.Glu1073_Lys1074insAlaArgGlu
NM_014795.3:c.3283_3291dup	NP_055610.1:p.Glu1097_Lys1098insAlaArgGlu
XM_006712881.2:c.3283_3291dup	XP_006712944.1:p.Glu1097_Lys1098insAlaArgGlu
XM_006712882.2:c.3283_3291dup	XP_006712945.1:p.Glu1097_Lys1098insAlaArgGlu
XM_011512231.1:c.3274_3282dup	XP_011510533.1:p.Glu1094_Lys1095insAlaArgGlu
XM_011512232.1:c.3262_3270dup	XP_011510534.1:p.Glu1090_Lys1091insAlaArgGlu
NM_014795.4:c.3283_3291dup MANE Select	NP_055610.1:p.Glu1097_Lys1098insAlaArgGlu
NM_001171653.2:c.3211_3219dup	NP_001165124.1:p.Glu1073_Lys1074insAlaArgGlu