Canonical Allele Identifier: CA348698655

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147067A>C (hg19) ; chr2:g.144389500A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389500A>C , CM000664.2:g.144389500A>C	GRCh38
NC_000002.11:g.145147067A>C , CM000664.1:g.145147067A>C	GRCh37
NC_000002.10:g.144863537A>C	NCBI36
NG_016431.1:g.135892T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3445T>G	ENSP00000508434.1:n.*3445T>G
ENST00000440875.6:c.2819T>G	ENSP00000475553.3:p.Met940Arg
ENST00000627532.3:c.3596T>G MANE Select	ENSP00000487174.1:p.Met1199Arg
ENST00000636026.2:c.3484T>G	ENSP00000490776.1:p.Trp1162Gly
ENST00000636179.1:n.3565T>G
ENST00000636413.1:c.3260T>G	ENSP00000490508.1:p.Met1087Arg
ENST00000636471.1:c.3671T>G	ENSP00000490317.1:p.Met1224Arg
ENST00000636732.2:c.*3313T>G	ENSP00000490175.1:n.*3313T>G
ENST00000636820.1:n.3696T>G
ENST00000637045.1:c.3260T>G	ENSP00000490141.1:p.Met1087Arg
ENST00000637304.1:c.3260T>G	ENSP00000490872.1:p.Met1087Arg
ENST00000638007.1:c.3260T>G	ENSP00000490723.1:p.Met1087Arg
ENST00000638087.1:c.3260T>G	ENSP00000490673.1:p.Met1087Arg
ENST00000638128.1:c.2819T>G	ENSP00000490934.1:p.Met940Arg
ENST00000639389.1:c.151+6912T>G	ENSP00000492572.1:n.151+6912T>G
ENST00000647488.1:c.816T>G	ENSP00000494820.1:n.816T>G
ENST00000675069.1:c.1127T>G	ENSP00000502467.1:p.Met376Arg
ENST00000303660.8:c.3593T>G	ENSP00000302501.4:p.Met1198Arg
ENST00000409487.7:c.3596T>G	ENSP00000386854.2:p.Met1199Arg
ENST00000419938.5:c.656-618T>G	ENSP00000394777.2:n.656-618T>G
ENST00000539609.7:c.3524T>G	ENSP00000443792.2:p.Met1175Arg
ENST00000558170.6:c.3596T>G	ENSP00000454157.1:p.Met1199Arg
ENST00000627532.2:c.3596T>G	ENSP00000487174.1:p.Met1199Arg
NM_001171653.1:c.3524T>G	NP_001165124.1:p.Met1175Arg
NM_014795.3:c.3596T>G	NP_055610.1:p.Met1199Arg
XM_006712881.2:c.3596T>G	XP_006712944.1:p.Met1199Arg
XM_006712882.2:c.3596T>G	XP_006712945.1:p.Met1199Arg
XM_011512231.1:c.3587T>G	XP_011510533.1:p.Met1196Arg
XM_011512232.1:c.3575T>G	XP_011510534.1:p.Met1192Arg
NM_014795.4:c.3596T>G MANE Select	NP_055610.1:p.Met1199Arg
NM_001171653.2:c.3524T>G	NP_001165124.1:p.Met1175Arg