Canonical Allele Identifier: CA348714711

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161556A>C (hg19) ; chr2:g.144403989A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403989A>C , CM000664.2:g.144403989A>C	GRCh38
NC_000002.11:g.145161556A>C , CM000664.1:g.145161556A>C	GRCh37
NC_000002.10:g.144878026A>C	NCBI36
NG_016431.1:g.121403T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*583T>G	ENSP00000508434.1:n.*583T>G
ENST00000440875.6:c.-44T>G	ENSP00000475553.3:n.-44T>G
ENST00000627532.3:c.734T>G MANE Select	ENSP00000487174.1:p.Leu245Arg
ENST00000636026.2:c.734T>G	ENSP00000490776.1:p.Leu245Arg
ENST00000636179.1:n.703T>G
ENST00000636413.1:c.398T>G	ENSP00000490508.1:p.Leu133Arg
ENST00000636471.1:c.734T>G	ENSP00000490317.1:p.Leu245Arg
ENST00000636732.2:c.*451T>G	ENSP00000490175.1:n.*451T>G
ENST00000636820.1:n.834T>G
ENST00000637045.1:c.398T>G	ENSP00000490141.1:p.Leu133Arg
ENST00000637267.2:c.734T>G	ENSP00000490293.2:p.Leu245Arg
ENST00000637304.1:c.398T>G	ENSP00000490872.1:p.Leu133Arg
ENST00000638007.1:c.398T>G	ENSP00000490723.1:p.Leu133Arg
ENST00000638087.1:c.398T>G	ENSP00000490673.1:p.Leu133Arg
ENST00000638128.1:c.-44T>G	ENSP00000490934.1:n.-44T>G
ENST00000675069.1:c.-133-5139T>G	ENSP00000502467.1:n.-133-5139T>G
ENST00000303660.8:c.731T>G	ENSP00000302501.4:p.Leu244Arg
ENST00000392861.6:c.818T>G	ENSP00000376601.3:p.Leu273Arg
ENST00000409487.7:c.734T>G	ENSP00000386854.2:p.Leu245Arg
ENST00000419938.5:c.473T>G	ENSP00000394777.2:p.Leu158Arg
ENST00000427902.5:c.821T>G	ENSP00000395496.2:p.Leu274Arg
ENST00000440875.5:c.719T>G	ENSP00000475553.2:p.Leu240Arg
ENST00000539609.7:c.662T>G	ENSP00000443792.2:p.Leu221Arg
ENST00000558170.6:c.734T>G	ENSP00000454157.1:p.Leu245Arg
ENST00000627532.2:c.734T>G	ENSP00000487174.1:p.Leu245Arg
NM_001171653.1:c.662T>G	NP_001165124.1:p.Leu221Arg
NM_014795.3:c.734T>G	NP_055610.1:p.Leu245Arg
XM_006712881.2:c.734T>G	XP_006712944.1:p.Leu245Arg
XM_006712882.2:c.734T>G	XP_006712945.1:p.Leu245Arg
XM_011512231.1:c.725T>G	XP_011510533.1:p.Leu242Arg
XM_011512232.1:c.713T>G	XP_011510534.1:p.Leu238Arg
NM_014795.4:c.734T>G MANE Select	NP_055610.1:p.Leu245Arg
NM_001171653.2:c.662T>G	NP_001165124.1:p.Leu221Arg