Canonical Allele Identifier: CA348701837

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147592T>G (hg19) ; chr2:g.144390025T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144390025T>G , CM000664.2:g.144390025T>G	GRCh38
NC_000002.11:g.145147592T>G , CM000664.1:g.145147592T>G	GRCh37
NC_000002.10:g.144864062T>G	NCBI36
NG_016431.1:g.135367A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2920A>C	ENSP00000508434.1:n.*2920A>C
ENST00000440875.6:c.2294A>C	ENSP00000475553.3:p.Lys765Thr
ENST00000627532.3:c.3071A>C MANE Select	ENSP00000487174.1:p.Lys1024Thr
ENST00000636026.2:c.3071A>C	ENSP00000490776.1:p.Lys1024Thr
ENST00000636179.1:n.3040A>C
ENST00000636413.1:c.2735A>C	ENSP00000490508.1:p.Lys912Thr
ENST00000636471.1:c.3146A>C	ENSP00000490317.1:p.Lys1049Thr
ENST00000636732.2:c.*2788A>C	ENSP00000490175.1:n.*2788A>C
ENST00000636820.1:n.3171A>C
ENST00000637045.1:c.2735A>C	ENSP00000490141.1:p.Lys912Thr
ENST00000637304.1:c.2735A>C	ENSP00000490872.1:p.Lys912Thr
ENST00000638007.1:c.2735A>C	ENSP00000490723.1:p.Lys912Thr
ENST00000638087.1:c.2735A>C	ENSP00000490673.1:p.Lys912Thr
ENST00000638128.1:c.2294A>C	ENSP00000490934.1:p.Lys765Thr
ENST00000639389.1:c.151+6387A>C	ENSP00000492572.1:n.151+6387A>C
ENST00000647488.1:c.291A>C	ENSP00000494820.1:n.291A>C
ENST00000675069.1:c.602A>C	ENSP00000502467.1:p.Lys201Thr
ENST00000303660.8:c.3068A>C	ENSP00000302501.4:p.Lys1023Thr
ENST00000409487.7:c.3071A>C	ENSP00000386854.2:p.Lys1024Thr
ENST00000419938.5:c.656-1143A>C	ENSP00000394777.2:n.656-1143A>C
ENST00000539609.7:c.2999A>C	ENSP00000443792.2:p.Lys1000Thr
ENST00000558170.6:c.3071A>C	ENSP00000454157.1:p.Lys1024Thr
ENST00000627532.2:c.3071A>C	ENSP00000487174.1:p.Lys1024Thr
NM_001171653.1:c.2999A>C	NP_001165124.1:p.Lys1000Thr
NM_014795.3:c.3071A>C	NP_055610.1:p.Lys1024Thr
XM_006712881.2:c.3071A>C	XP_006712944.1:p.Lys1024Thr
XM_006712882.2:c.3071A>C	XP_006712945.1:p.Lys1024Thr
XM_011512231.1:c.3062A>C	XP_011510533.1:p.Lys1021Thr
XM_011512232.1:c.3050A>C	XP_011510534.1:p.Lys1017Thr
NM_014795.4:c.3071A>C MANE Select	NP_055610.1:p.Lys1024Thr
NM_001171653.2:c.2999A>C	NP_001165124.1:p.Lys1000Thr