Canonical Allele Identifier: CA348699238

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147196C>A (hg19) ; chr2:g.144389629C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389629C>A , CM000664.2:g.144389629C>A	GRCh38
NC_000002.11:g.145147196C>A , CM000664.1:g.145147196C>A	GRCh37
NC_000002.10:g.144863666C>A	NCBI36
NG_016431.1:g.135763G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3316G>T	ENSP00000508434.1:n.*3316G>T
ENST00000440875.6:c.2690G>T	ENSP00000475553.3:p.Gly897Val
ENST00000627532.3:c.3467G>T MANE Select	ENSP00000487174.1:p.Gly1156Val
ENST00000636026.2:c.3355G>T	ENSP00000490776.1:p.Ala1119Ser
ENST00000636179.1:n.3436G>T
ENST00000636413.1:c.3131G>T	ENSP00000490508.1:p.Gly1044Val
ENST00000636471.1:c.3542G>T	ENSP00000490317.1:p.Gly1181Val
ENST00000636732.2:c.*3184G>T	ENSP00000490175.1:n.*3184G>T
ENST00000636820.1:n.3567G>T
ENST00000637045.1:c.3131G>T	ENSP00000490141.1:p.Gly1044Val
ENST00000637304.1:c.3131G>T	ENSP00000490872.1:p.Gly1044Val
ENST00000638007.1:c.3131G>T	ENSP00000490723.1:p.Gly1044Val
ENST00000638087.1:c.3131G>T	ENSP00000490673.1:p.Gly1044Val
ENST00000638128.1:c.2690G>T	ENSP00000490934.1:p.Gly897Val
ENST00000639389.1:c.151+6783G>T	ENSP00000492572.1:n.151+6783G>T
ENST00000647488.1:c.687G>T	ENSP00000494820.1:n.687G>T
ENST00000675069.1:c.998G>T	ENSP00000502467.1:p.Gly333Val
ENST00000303660.8:c.3464G>T	ENSP00000302501.4:p.Gly1155Val
ENST00000409487.7:c.3467G>T	ENSP00000386854.2:p.Gly1156Val
ENST00000419938.5:c.656-747G>T	ENSP00000394777.2:n.656-747G>T
ENST00000539609.7:c.3395G>T	ENSP00000443792.2:p.Gly1132Val
ENST00000558170.6:c.3467G>T	ENSP00000454157.1:p.Gly1156Val
ENST00000627532.2:c.3467G>T	ENSP00000487174.1:p.Gly1156Val
NM_001171653.1:c.3395G>T	NP_001165124.1:p.Gly1132Val
NM_014795.3:c.3467G>T	NP_055610.1:p.Gly1156Val
XM_006712881.2:c.3467G>T	XP_006712944.1:p.Gly1156Val
XM_006712882.2:c.3467G>T	XP_006712945.1:p.Gly1156Val
XM_011512231.1:c.3458G>T	XP_011510533.1:p.Gly1153Val
XM_011512232.1:c.3446G>T	XP_011510534.1:p.Gly1149Val
NM_014795.4:c.3467G>T MANE Select	NP_055610.1:p.Gly1156Val
NM_001171653.2:c.3395G>T	NP_001165124.1:p.Gly1132Val