Canonical Allele Identifier: CA348699745

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147357T>G (hg19) ; chr2:g.144389790T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389790T>G , CM000664.2:g.144389790T>G	GRCh38
NC_000002.11:g.145147357T>G , CM000664.1:g.145147357T>G	GRCh37
NC_000002.10:g.144863827T>G	NCBI36
NG_016431.1:g.135602A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3155A>C	ENSP00000508434.1:n.*3155A>C
ENST00000440875.6:c.2529A>C	ENSP00000475553.3:p.Glu843Asp
ENST00000627532.3:c.3306A>C MANE Select	ENSP00000487174.1:p.Glu1102Asp
ENST00000636026.2:c.3231-37A>C	ENSP00000490776.1:n.3231-37A>C
ENST00000636179.1:n.3275A>C
ENST00000636413.1:c.2970A>C	ENSP00000490508.1:p.Glu990Asp
ENST00000636471.1:c.3381A>C	ENSP00000490317.1:p.Glu1127Asp
ENST00000636732.2:c.*3023A>C	ENSP00000490175.1:n.*3023A>C
ENST00000636820.1:n.3406A>C
ENST00000637045.1:c.2970A>C	ENSP00000490141.1:p.Glu990Asp
ENST00000637304.1:c.2970A>C	ENSP00000490872.1:p.Glu990Asp
ENST00000638007.1:c.2970A>C	ENSP00000490723.1:p.Glu990Asp
ENST00000638087.1:c.2970A>C	ENSP00000490673.1:p.Glu990Asp
ENST00000638128.1:c.2529A>C	ENSP00000490934.1:p.Glu843Asp
ENST00000639389.1:c.151+6622A>C	ENSP00000492572.1:n.151+6622A>C
ENST00000647488.1:c.526A>C	ENSP00000494820.1:n.526A>C
ENST00000675069.1:c.837A>C	ENSP00000502467.1:p.Glu279Asp
ENST00000303660.8:c.3303A>C	ENSP00000302501.4:p.Glu1101Asp
ENST00000409487.7:c.3306A>C	ENSP00000386854.2:p.Glu1102Asp
ENST00000419938.5:c.656-908A>C	ENSP00000394777.2:n.656-908A>C
ENST00000539609.7:c.3234A>C	ENSP00000443792.2:p.Glu1078Asp
ENST00000558170.6:c.3306A>C	ENSP00000454157.1:p.Glu1102Asp
ENST00000627532.2:c.3306A>C	ENSP00000487174.1:p.Glu1102Asp
NM_001171653.1:c.3234A>C	NP_001165124.1:p.Glu1078Asp
NM_014795.3:c.3306A>C	NP_055610.1:p.Glu1102Asp
XM_006712881.2:c.3306A>C	XP_006712944.1:p.Glu1102Asp
XM_006712882.2:c.3306A>C	XP_006712945.1:p.Glu1102Asp
XM_011512231.1:c.3297A>C	XP_011510533.1:p.Glu1099Asp
XM_011512232.1:c.3285A>C	XP_011510534.1:p.Glu1095Asp
NM_014795.4:c.3306A>C MANE Select	NP_055610.1:p.Glu1102Asp
NM_001171653.2:c.3234A>C	NP_001165124.1:p.Glu1078Asp