Canonical Allele Identifier: CA348699281

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147215T>G (hg19) ; chr2:g.144389648T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389648T>G , CM000664.2:g.144389648T>G	GRCh38
NC_000002.11:g.145147215T>G , CM000664.1:g.145147215T>G	GRCh37
NC_000002.10:g.144863685T>G	NCBI36
NG_016431.1:g.135744A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3297A>C	ENSP00000508434.1:n.*3297A>C
ENST00000440875.6:c.2671A>C	ENSP00000475553.3:p.Lys891Gln
ENST00000627532.3:c.3448A>C MANE Select	ENSP00000487174.1:p.Lys1150Gln
ENST00000636026.2:c.3336A>C	ENSP00000490776.1:p.Gly1112=
ENST00000636179.1:n.3417A>C
ENST00000636413.1:c.3112A>C	ENSP00000490508.1:p.Lys1038Gln
ENST00000636471.1:c.3523A>C	ENSP00000490317.1:p.Lys1175Gln
ENST00000636732.2:c.*3165A>C	ENSP00000490175.1:n.*3165A>C
ENST00000636820.1:n.3548A>C
ENST00000637045.1:c.3112A>C	ENSP00000490141.1:p.Lys1038Gln
ENST00000637304.1:c.3112A>C	ENSP00000490872.1:p.Lys1038Gln
ENST00000638007.1:c.3112A>C	ENSP00000490723.1:p.Lys1038Gln
ENST00000638087.1:c.3112A>C	ENSP00000490673.1:p.Lys1038Gln
ENST00000638128.1:c.2671A>C	ENSP00000490934.1:p.Lys891Gln
ENST00000639389.1:c.151+6764A>C	ENSP00000492572.1:n.151+6764A>C
ENST00000647488.1:c.668A>C	ENSP00000494820.1:n.668A>C
ENST00000675069.1:c.979A>C	ENSP00000502467.1:p.Lys327Gln
ENST00000303660.8:c.3445A>C	ENSP00000302501.4:p.Lys1149Gln
ENST00000409487.7:c.3448A>C	ENSP00000386854.2:p.Lys1150Gln
ENST00000419938.5:c.656-766A>C	ENSP00000394777.2:n.656-766A>C
ENST00000539609.7:c.3376A>C	ENSP00000443792.2:p.Lys1126Gln
ENST00000558170.6:c.3448A>C	ENSP00000454157.1:p.Lys1150Gln
ENST00000627532.2:c.3448A>C	ENSP00000487174.1:p.Lys1150Gln
NM_001171653.1:c.3376A>C	NP_001165124.1:p.Lys1126Gln
NM_014795.3:c.3448A>C	NP_055610.1:p.Lys1150Gln
XM_006712881.2:c.3448A>C	XP_006712944.1:p.Lys1150Gln
XM_006712882.2:c.3448A>C	XP_006712945.1:p.Lys1150Gln
XM_011512231.1:c.3439A>C	XP_011510533.1:p.Lys1147Gln
XM_011512232.1:c.3427A>C	XP_011510534.1:p.Lys1143Gln
NM_014795.4:c.3448A>C MANE Select	NP_055610.1:p.Lys1150Gln
NM_001171653.2:c.3376A>C	NP_001165124.1:p.Lys1126Gln