Canonical Allele Identifier: CA10612339

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 331286
• ClinVar RCV Id: RCV000336653
• dbSNP Id: rs534438826
• gnomAD v2: 2-145145898-GCTCTT-G
• gnomAD v3: 2-144388331-GCTCTT-G
• gnomAD v4: 2-144388331-GCTCTT-G
• MyVariant Identifiers: chr2:g.145145899_145145903del (hg19) ; chr2:g.144388332_144388336del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144388337_144388341del , CM000664.2:g.144388337_144388341del	GRCh38
NC_000002.11:g.145145904_145145908del , CM000664.1:g.145145904_145145908del	GRCh37
NC_000002.10:g.144862374_144862378del	NCBI36
NG_016431.1:g.137056_137060del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440875.6:c.*1115_*1119del	ENSP00000475553.3:n.*1115_*1119del
ENST00000627532.3:c.*1115_*1119del MANE Select	ENSP00000487174.1:n.*1115_*1119del
ENST00000636179.1:n.4729_4733del
ENST00000636413.1:c.*1115_*1119del	ENSP00000490508.1:n.*1115_*1119del
ENST00000636471.1:c.*1115_*1119del	ENSP00000490317.1:n.*1115_*1119del
ENST00000636732.2:c.*4477_*4481del	ENSP00000490175.1:n.*4477_*4481del
ENST00000636820.1:n.4860_4864del
ENST00000637045.1:c.*1115_*1119del	ENSP00000490141.1:n.*1115_*1119del
ENST00000637304.1:c.*1115_*1119del	ENSP00000490872.1:n.*1115_*1119del
ENST00000638007.1:c.*1115_*1119del	ENSP00000490723.1:n.*1115_*1119del
ENST00000638087.1:c.*1115_*1119del	ENSP00000490673.1:n.*1115_*1119del
ENST00000638128.1:c.*1115_*1119del	ENSP00000490934.1:n.*1115_*1119del
ENST00000639389.1:c.151+8076_151+8080del	ENSP00000492572.1:n.151+8076_151+8080del
ENST00000409487.7:c.*1115_*1119del	ENSP00000386854.2:n.*1115_*1119del
ENST00000419938.5:c.*539_*543del	ENSP00000394777.2:n.*539_*543del
ENST00000627532.2:c.*1115_*1119del	ENSP00000487174.1:n.*1115_*1119del
NM_001171653.1:c.*1115_*1119del	NP_001165124.1:n.*1115_*1119del
NM_014795.3:c.*1115_*1119del	NP_055610.1:n.*1115_*1119del
XM_006712881.2:c.*1115_*1119del	XP_006712944.1:n.*1115_*1119del
XM_006712882.2:c.*1115_*1119del	XP_006712945.1:n.*1115_*1119del
XM_011512231.1:c.*1115_*1119del	XP_011510533.1:n.*1115_*1119del
XM_011512232.1:c.*1115_*1119del	XP_011510534.1:n.*1115_*1119del
NM_014795.4:c.*1115_*1119del MANE Select	NP_055610.1:n.*1115_*1119del
NM_001171653.2:c.*1115_*1119del	NP_001165124.1:n.*1115_*1119del