Canonical Allele Identifier: CA348699065

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1346793
• ClinVar RCV Id: RCV002030188
• dbSNP Id: rs1238900874
• MyVariant Identifiers: chr2:g.145147127A>T (hg19) ; chr2:g.144389560A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389560A>T , CM000664.2:g.144389560A>T	GRCh38
NC_000002.11:g.145147127A>T , CM000664.1:g.145147127A>T	GRCh37
NC_000002.10:g.144863597A>T	NCBI36
NG_016431.1:g.135832T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3385T>A	ENSP00000508434.1:n.*3385T>A
ENST00000440875.6:c.2759T>A	ENSP00000475553.3:p.Ile920Lys
ENST00000627532.3:c.3536T>A MANE Select	ENSP00000487174.1:p.Ile1179Lys
ENST00000636026.2:c.3424T>A	ENSP00000490776.1:p.Tyr1142Asn
ENST00000636179.1:n.3505T>A
ENST00000636413.1:c.3200T>A	ENSP00000490508.1:p.Ile1067Lys
ENST00000636471.1:c.3611T>A	ENSP00000490317.1:p.Ile1204Lys
ENST00000636732.2:c.*3253T>A	ENSP00000490175.1:n.*3253T>A
ENST00000636820.1:n.3636T>A
ENST00000637045.1:c.3200T>A	ENSP00000490141.1:p.Ile1067Lys
ENST00000637304.1:c.3200T>A	ENSP00000490872.1:p.Ile1067Lys
ENST00000638007.1:c.3200T>A	ENSP00000490723.1:p.Ile1067Lys
ENST00000638087.1:c.3200T>A	ENSP00000490673.1:p.Ile1067Lys
ENST00000638128.1:c.2759T>A	ENSP00000490934.1:p.Ile920Lys
ENST00000639389.1:c.151+6852T>A	ENSP00000492572.1:n.151+6852T>A
ENST00000647488.1:c.756T>A	ENSP00000494820.1:n.756T>A
ENST00000675069.1:c.1067T>A	ENSP00000502467.1:p.Ile356Lys
ENST00000303660.8:c.3533T>A	ENSP00000302501.4:p.Ile1178Lys
ENST00000409487.7:c.3536T>A	ENSP00000386854.2:p.Ile1179Lys
ENST00000419938.5:c.656-678T>A	ENSP00000394777.2:n.656-678T>A
ENST00000539609.7:c.3464T>A	ENSP00000443792.2:p.Ile1155Lys
ENST00000558170.6:c.3536T>A	ENSP00000454157.1:p.Ile1179Lys
ENST00000627532.2:c.3536T>A	ENSP00000487174.1:p.Ile1179Lys
NM_001171653.1:c.3464T>A	NP_001165124.1:p.Ile1155Lys
NM_014795.3:c.3536T>A	NP_055610.1:p.Ile1179Lys
XM_006712881.2:c.3536T>A	XP_006712944.1:p.Ile1179Lys
XM_006712882.2:c.3536T>A	XP_006712945.1:p.Ile1179Lys
XM_011512231.1:c.3527T>A	XP_011510533.1:p.Ile1176Lys
XM_011512232.1:c.3515T>A	XP_011510534.1:p.Ile1172Lys
NM_014795.4:c.3536T>A MANE Select	NP_055610.1:p.Ile1179Lys
NM_001171653.2:c.3464T>A	NP_001165124.1:p.Ile1155Lys