Canonical Allele Identifier: CA348699106

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147145T>C (hg19) ; chr2:g.144389578T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389578T>C , CM000664.2:g.144389578T>C	GRCh38
NC_000002.11:g.145147145T>C , CM000664.1:g.145147145T>C	GRCh37
NC_000002.10:g.144863615T>C	NCBI36
NG_016431.1:g.135814A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3367A>G	ENSP00000508434.1:n.*3367A>G
ENST00000440875.6:c.2741A>G	ENSP00000475553.3:p.Asp914Gly
ENST00000627532.3:c.3518A>G MANE Select	ENSP00000487174.1:p.Asp1173Gly
ENST00000636026.2:c.3406A>G	ENSP00000490776.1:p.Ile1136Val
ENST00000636179.1:n.3487A>G
ENST00000636413.1:c.3182A>G	ENSP00000490508.1:p.Asp1061Gly
ENST00000636471.1:c.3593A>G	ENSP00000490317.1:p.Asp1198Gly
ENST00000636732.2:c.*3235A>G	ENSP00000490175.1:n.*3235A>G
ENST00000636820.1:n.3618A>G
ENST00000637045.1:c.3182A>G	ENSP00000490141.1:p.Asp1061Gly
ENST00000637304.1:c.3182A>G	ENSP00000490872.1:p.Asp1061Gly
ENST00000638007.1:c.3182A>G	ENSP00000490723.1:p.Asp1061Gly
ENST00000638087.1:c.3182A>G	ENSP00000490673.1:p.Asp1061Gly
ENST00000638128.1:c.2741A>G	ENSP00000490934.1:p.Asp914Gly
ENST00000639389.1:c.151+6834A>G	ENSP00000492572.1:n.151+6834A>G
ENST00000647488.1:c.738A>G	ENSP00000494820.1:n.738A>G
ENST00000675069.1:c.1049A>G	ENSP00000502467.1:p.Asp350Gly
ENST00000303660.8:c.3515A>G	ENSP00000302501.4:p.Asp1172Gly
ENST00000409487.7:c.3518A>G	ENSP00000386854.2:p.Asp1173Gly
ENST00000419938.5:c.656-696A>G	ENSP00000394777.2:n.656-696A>G
ENST00000539609.7:c.3446A>G	ENSP00000443792.2:p.Asp1149Gly
ENST00000558170.6:c.3518A>G	ENSP00000454157.1:p.Asp1173Gly
ENST00000627532.2:c.3518A>G	ENSP00000487174.1:p.Asp1173Gly
NM_001171653.1:c.3446A>G	NP_001165124.1:p.Asp1149Gly
NM_014795.3:c.3518A>G	NP_055610.1:p.Asp1173Gly
XM_006712881.2:c.3518A>G	XP_006712944.1:p.Asp1173Gly
XM_006712882.2:c.3518A>G	XP_006712945.1:p.Asp1173Gly
XM_011512231.1:c.3509A>G	XP_011510533.1:p.Asp1170Gly
XM_011512232.1:c.3497A>G	XP_011510534.1:p.Asp1166Gly
NM_014795.4:c.3518A>G MANE Select	NP_055610.1:p.Asp1173Gly
NM_001171653.2:c.3446A>G	NP_001165124.1:p.Asp1149Gly