Canonical Allele Identifier: CA2739271219

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2810828
• ClinVar RCV Id: RCV003612649

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389883_144389884insCC , CM000664.2:g.144389883_144389884insCC	GRCh38
NC_000002.11:g.145147450_145147451insCC , CM000664.1:g.145147450_145147451insCC	GRCh37
NC_000002.10:g.144863920_144863921insCC	NCBI36
NG_016431.1:g.135509_135510insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3062_*3063insGG	ENSP00000508434.1:n.*3062_*3063insGG
ENST00000440875.6:c.2436_2437insGG	ENSP00000475553.3:p.Gln813GlyfsTer4
ENST00000627532.3:c.3213_3214insGG MANE Select	ENSP00000487174.1:p.Gln1072GlyfsTer4
ENST00000636026.2:c.3213_3214insGG	ENSP00000490776.1:p.Gln1072GlyfsTer4
ENST00000636179.1:n.3182_3183insGG
ENST00000636413.1:c.2877_2878insGG	ENSP00000490508.1:p.Gln960GlyfsTer4
ENST00000636471.1:c.3288_3289insGG	ENSP00000490317.1:p.Gln1097GlyfsTer4
ENST00000636732.2:c.*2930_*2931insGG	ENSP00000490175.1:n.*2930_*2931insGG
ENST00000636820.1:n.3313_3314insGG
ENST00000637045.1:c.2877_2878insGG	ENSP00000490141.1:p.Gln960GlyfsTer4
ENST00000637304.1:c.2877_2878insGG	ENSP00000490872.1:p.Gln960GlyfsTer4
ENST00000638007.1:c.2877_2878insGG	ENSP00000490723.1:p.Gln960GlyfsTer4
ENST00000638087.1:c.2877_2878insGG	ENSP00000490673.1:p.Gln960GlyfsTer4
ENST00000638128.1:c.2436_2437insGG	ENSP00000490934.1:p.Gln813GlyfsTer4
ENST00000639389.1:c.151+6529_151+6530insGG	ENSP00000492572.1:n.151+6529_151+6530insGG
ENST00000647488.1:c.433_434insGG	ENSP00000494820.1:n.433_434insGG
ENST00000675069.1:c.744_745insGG	ENSP00000502467.1:p.Gln249GlyfsTer4
ENST00000303660.8:c.3210_3211insGG	ENSP00000302501.4:p.Gln1071GlyfsTer4
ENST00000409487.7:c.3213_3214insGG	ENSP00000386854.2:p.Gln1072GlyfsTer4
ENST00000419938.5:c.656-1001_656-1000insGG	ENSP00000394777.2:n.656-1001_656-1000insGG
ENST00000539609.7:c.3141_3142insGG	ENSP00000443792.2:p.Gln1048GlyfsTer4
ENST00000558170.6:c.3213_3214insGG	ENSP00000454157.1:p.Gln1072GlyfsTer4
ENST00000627532.2:c.3213_3214insGG	ENSP00000487174.1:p.Gln1072GlyfsTer4
NM_001171653.1:c.3141_3142insGG	NP_001165124.1:p.Gln1048GlyfsTer4
NM_014795.3:c.3213_3214insGG	NP_055610.1:p.Gln1072GlyfsTer4
XM_006712881.2:c.3213_3214insGG	XP_006712944.1:p.Gln1072GlyfsTer4
XM_006712882.2:c.3213_3214insGG	XP_006712945.1:p.Gln1072GlyfsTer4
XM_011512231.1:c.3204_3205insGG	XP_011510533.1:p.Gln1069GlyfsTer4
XM_011512232.1:c.3192_3193insGG	XP_011510534.1:p.Gln1065GlyfsTer4
NM_014795.4:c.3213_3214insGG MANE Select	NP_055610.1:p.Gln1072GlyfsTer4
NM_001171653.2:c.3141_3142insGG	NP_001165124.1:p.Gln1048GlyfsTer4