Canonical Allele Identifier: CA348700070

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147424T>G (hg19) ; chr2:g.144389857T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389857T>G , CM000664.2:g.144389857T>G	GRCh38
NC_000002.11:g.145147424T>G , CM000664.1:g.145147424T>G	GRCh37
NC_000002.10:g.144863894T>G	NCBI36
NG_016431.1:g.135535A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3088A>C	ENSP00000508434.1:n.*3088A>C
ENST00000440875.6:c.2462A>C	ENSP00000475553.3:p.Tyr821Ser
ENST00000627532.3:c.3239A>C MANE Select	ENSP00000487174.1:p.Tyr1080Ser
ENST00000636026.2:c.3230+9A>C	ENSP00000490776.1:n.3230+9A>C
ENST00000636179.1:n.3208A>C
ENST00000636413.1:c.2903A>C	ENSP00000490508.1:p.Tyr968Ser
ENST00000636471.1:c.3314A>C	ENSP00000490317.1:p.Tyr1105Ser
ENST00000636732.2:c.*2956A>C	ENSP00000490175.1:n.*2956A>C
ENST00000636820.1:n.3339A>C
ENST00000637045.1:c.2903A>C	ENSP00000490141.1:p.Tyr968Ser
ENST00000637304.1:c.2903A>C	ENSP00000490872.1:p.Tyr968Ser
ENST00000638007.1:c.2903A>C	ENSP00000490723.1:p.Tyr968Ser
ENST00000638087.1:c.2903A>C	ENSP00000490673.1:p.Tyr968Ser
ENST00000638128.1:c.2462A>C	ENSP00000490934.1:p.Tyr821Ser
ENST00000639389.1:c.151+6555A>C	ENSP00000492572.1:n.151+6555A>C
ENST00000647488.1:c.459A>C	ENSP00000494820.1:n.459A>C
ENST00000675069.1:c.770A>C	ENSP00000502467.1:p.Tyr257Ser
ENST00000303660.8:c.3236A>C	ENSP00000302501.4:p.Tyr1079Ser
ENST00000409487.7:c.3239A>C	ENSP00000386854.2:p.Tyr1080Ser
ENST00000419938.5:c.656-975A>C	ENSP00000394777.2:n.656-975A>C
ENST00000539609.7:c.3167A>C	ENSP00000443792.2:p.Tyr1056Ser
ENST00000558170.6:c.3239A>C	ENSP00000454157.1:p.Tyr1080Ser
ENST00000627532.2:c.3239A>C	ENSP00000487174.1:p.Tyr1080Ser
NM_001171653.1:c.3167A>C	NP_001165124.1:p.Tyr1056Ser
NM_014795.3:c.3239A>C	NP_055610.1:p.Tyr1080Ser
XM_006712881.2:c.3239A>C	XP_006712944.1:p.Tyr1080Ser
XM_006712882.2:c.3239A>C	XP_006712945.1:p.Tyr1080Ser
XM_011512231.1:c.3230A>C	XP_011510533.1:p.Tyr1077Ser
XM_011512232.1:c.3218A>C	XP_011510534.1:p.Tyr1073Ser
NM_014795.4:c.3239A>C MANE Select	NP_055610.1:p.Tyr1080Ser
NM_001171653.2:c.3167A>C	NP_001165124.1:p.Tyr1056Ser