Canonical Allele Identifier: CA10610843

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 331292
• ClinVar RCV Id: RCV000364159
• dbSNP Id: rs558553086
• gnomAD v2: 2-145146503-GA-G
• gnomAD v3: 2-144388936-GA-G
• gnomAD v4: 2-144388936-GA-G
• MyVariant Identifiers: chr2:g.145146504del (hg19) ; chr2:g.144388937del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144388946del , CM000664.2:g.144388946del	GRCh38
NC_000002.11:g.145146513del , CM000664.1:g.145146513del	GRCh37
NC_000002.10:g.144862983del	NCBI36
NG_016431.1:g.136455del

Transcript Alleles

HGVS	Amino-acid change
ENST00000440875.6:c.*514del	ENSP00000475553.3:n.*514del
ENST00000627532.3:c.*514del MANE Select	ENSP00000487174.1:n.*514del
ENST00000636026.2:c.*438del	ENSP00000490776.1:n.*438del
ENST00000636179.1:n.4128del
ENST00000636413.1:c.*514del	ENSP00000490508.1:n.*514del
ENST00000636471.1:c.*514del	ENSP00000490317.1:n.*514del
ENST00000636732.2:c.*3876del	ENSP00000490175.1:n.*3876del
ENST00000636820.1:n.4259del
ENST00000637045.1:c.*514del	ENSP00000490141.1:n.*514del
ENST00000637304.1:c.*514del	ENSP00000490872.1:n.*514del
ENST00000638007.1:c.*514del	ENSP00000490723.1:n.*514del
ENST00000638087.1:c.*514del	ENSP00000490673.1:n.*514del
ENST00000638128.1:c.*514del	ENSP00000490934.1:n.*514del
ENST00000639389.1:c.151+7475del	ENSP00000492572.1:n.151+7475del
ENST00000647488.1:c.1379del	ENSP00000494820.1:n.1379del
ENST00000675069.1:c.*514del	ENSP00000502467.1:n.*514del
ENST00000409487.7:c.*514del	ENSP00000386854.2:n.*514del
ENST00000419938.5:c.656-55del	ENSP00000394777.2:n.656-55del
ENST00000627532.2:c.*514del	ENSP00000487174.1:n.*514del
NM_001171653.1:c.*514del	NP_001165124.1:n.*514del
NM_014795.3:c.*514del	NP_055610.1:n.*514del
XM_006712881.2:c.*514del	XP_006712944.1:n.*514del
XM_006712882.2:c.*514del	XP_006712945.1:n.*514del
XM_011512231.1:c.*514del	XP_011510533.1:n.*514del
XM_011512232.1:c.*514del	XP_011510534.1:n.*514del
NM_014795.4:c.*514del MANE Select	NP_055610.1:n.*514del
NM_001171653.2:c.*514del	NP_001165124.1:n.*514del