Canonical Allele Identifier: CA267214

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 95638
• ClinVar RCV Id: RCV000081672 ; RCV000850621
• dbSNP Id: rs398124281
• MyVariant Identifiers: chr2:g.145161631_145161647del (hg19) ; chr2:g.145161631_145161647delTAGCCCCGGTCGCAGTA (hg19) ; chr2:g.144404064_144404080del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404064_144404080del , CM000664.2:g.144404064_144404080del	GRCh38
NC_000002.11:g.145161631_145161647del , CM000664.1:g.145161631_145161647del	GRCh37
NC_000002.10:g.144878101_144878117del	NCBI36
NG_016431.1:g.121312_121328del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*492_*508del	ENSP00000508434.1:n.*492_*508del
ENST00000440875.6:c.-135_-119del	ENSP00000475553.3:n.-135_-119del
ENST00000627532.3:c.643_659del MANE Select	ENSP00000487174.1:p.Tyr215GlnfsTer18
ENST00000636026.2:c.643_659del	ENSP00000490776.1:p.Tyr215GlnfsTer18
ENST00000636179.1:n.612_628del
ENST00000636413.1:c.307_323del	ENSP00000490508.1:p.Tyr103GlnfsTer18
ENST00000636471.1:c.643_659del	ENSP00000490317.1:p.Tyr215GlnfsTer18
ENST00000636732.2:c.*360_*376del	ENSP00000490175.1:n.*360_*376del
ENST00000636820.1:n.743_759del
ENST00000637045.1:c.307_323del	ENSP00000490141.1:p.Tyr103GlnfsTer18
ENST00000637267.2:c.643_659del	ENSP00000490293.2:p.Tyr215GlnfsTer18
ENST00000637304.1:c.307_323del	ENSP00000490872.1:p.Tyr103GlnfsTer18
ENST00000638007.1:c.307_323del	ENSP00000490723.1:p.Tyr103GlnfsTer18
ENST00000638087.1:c.307_323del	ENSP00000490673.1:p.Tyr103GlnfsTer18
ENST00000638128.1:c.-135_-119del	ENSP00000490934.1:n.-135_-119del
ENST00000675069.1:c.-133-5230_-133-5214del	ENSP00000502467.1:n.-133-5230_-133-5214del
ENST00000303660.8:c.640_656del	ENSP00000302501.4:p.Tyr214GlnfsTer18
ENST00000392861.6:c.727_743del	ENSP00000376601.3:p.Tyr243GlnfsTer18
ENST00000409487.7:c.643_659del	ENSP00000386854.2:p.Tyr215GlnfsTer18
ENST00000419938.5:c.382_398del	ENSP00000394777.2:p.Tyr128GlnfsTer18
ENST00000427902.5:c.730_746del	ENSP00000395496.2:p.Tyr244GlnfsTer18
ENST00000440875.5:c.628_644del	ENSP00000475553.2:p.Tyr210GlnfsTer18
ENST00000497268.1:n.589_605del
ENST00000539609.7:c.571_587del	ENSP00000443792.2:p.Tyr191GlnfsTer18
ENST00000558170.6:c.643_659del	ENSP00000454157.1:p.Tyr215GlnfsTer18
ENST00000627532.2:c.643_659del	ENSP00000487174.1:p.Tyr215GlnfsTer18
NM_001171653.1:c.571_587del	NP_001165124.1:p.Tyr191GlnfsTer18
NM_014795.3:c.643_659del	NP_055610.1:p.Tyr215GlnfsTer18
XM_006712881.2:c.643_659del	XP_006712944.1:p.Tyr215GlnfsTer18
XM_006712882.2:c.643_659del	XP_006712945.1:p.Tyr215GlnfsTer18
XM_011512231.1:c.634_650del	XP_011510533.1:p.Tyr212GlnfsTer18
XM_011512232.1:c.622_638del	XP_011510534.1:p.Tyr208GlnfsTer18
NM_014795.4:c.643_659del MANE Select	NP_055610.1:p.Tyr215GlnfsTer18
NM_001171653.2:c.571_587del	NP_001165124.1:p.Tyr191GlnfsTer18