Canonical Allele Identifier: CA348711349

Gene: ZEB2

Linked Data

• dbSNP Id: rs1382650872
• gnomAD v3: 2-144399730-A-G
• gnomAD v4: 2-144399730-A-G
• MyVariant Identifiers: chr2:g.145157297A>G (hg19) ; chr2:g.144399730A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399730A>G , CM000664.2:g.144399730A>G	GRCh38
NC_000002.11:g.145157297A>G , CM000664.1:g.145157297A>G	GRCh37
NC_000002.10:g.144873767A>G	NCBI36
NG_016431.1:g.125662T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1306T>C	ENSP00000508434.1:n.*1306T>C
ENST00000440875.6:c.680T>C	ENSP00000475553.3:p.Leu227Ser
ENST00000627532.3:c.1457T>C MANE Select	ENSP00000487174.1:p.Leu486Ser
ENST00000636026.2:c.1457T>C	ENSP00000490776.1:p.Leu486Ser
ENST00000636179.1:n.1426T>C
ENST00000636413.1:c.1121T>C	ENSP00000490508.1:p.Leu374Ser
ENST00000636471.1:c.1532T>C	ENSP00000490317.1:p.Leu511Ser
ENST00000636732.2:c.*1174T>C	ENSP00000490175.1:n.*1174T>C
ENST00000636820.1:n.1557T>C
ENST00000637045.1:c.1121T>C	ENSP00000490141.1:p.Leu374Ser
ENST00000637267.2:c.1457T>C	ENSP00000490293.2:p.Leu486Ser
ENST00000637304.1:c.1121T>C	ENSP00000490872.1:p.Leu374Ser
ENST00000638007.1:c.1121T>C	ENSP00000490723.1:p.Leu374Ser
ENST00000638087.1:c.1121T>C	ENSP00000490673.1:p.Leu374Ser
ENST00000638128.1:c.680T>C	ENSP00000490934.1:p.Leu227Ser
ENST00000675069.1:c.-133-880T>C	ENSP00000502467.1:n.-133-880T>C
ENST00000675145.1:n.2005T>C
ENST00000303660.8:c.1454T>C	ENSP00000302501.4:p.Leu485Ser
ENST00000409487.7:c.1457T>C	ENSP00000386854.2:p.Leu486Ser
ENST00000419938.5:c.655+1469T>C	ENSP00000394777.2:n.655+1469T>C
ENST00000427902.5:c.1544T>C	ENSP00000395496.2:p.Leu515Ser
ENST00000440875.5:c.1154-180T>C	ENSP00000475553.2:n.1154-180T>C
ENST00000539609.7:c.1385T>C	ENSP00000443792.2:p.Leu462Ser
ENST00000558170.6:c.1457T>C	ENSP00000454157.1:p.Leu486Ser
ENST00000627532.2:c.1457T>C	ENSP00000487174.1:p.Leu486Ser
NM_001171653.1:c.1385T>C	NP_001165124.1:p.Leu462Ser
NM_014795.3:c.1457T>C	NP_055610.1:p.Leu486Ser
XM_006712881.2:c.1457T>C	XP_006712944.1:p.Leu486Ser
XM_006712882.2:c.1457T>C	XP_006712945.1:p.Leu486Ser
XM_011512231.1:c.1448T>C	XP_011510533.1:p.Leu483Ser
XM_011512232.1:c.1436T>C	XP_011510534.1:p.Leu479Ser
NM_014795.4:c.1457T>C MANE Select	NP_055610.1:p.Leu486Ser
NM_001171653.2:c.1385T>C	NP_001165124.1:p.Leu462Ser