Canonical Allele Identifier: CA348700453

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147469G>T (hg19) ; chr2:g.144389902G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389902G>T , CM000664.2:g.144389902G>T	GRCh38
NC_000002.11:g.145147469G>T , CM000664.1:g.145147469G>T	GRCh37
NC_000002.10:g.144863939G>T	NCBI36
NG_016431.1:g.135490C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3043C>A	ENSP00000508434.1:n.*3043C>A
ENST00000440875.6:c.2417C>A	ENSP00000475553.3:p.Ser806Ter
ENST00000627532.3:c.3194C>A MANE Select	ENSP00000487174.1:p.Ser1065Ter
ENST00000636026.2:c.3194C>A	ENSP00000490776.1:p.Ser1065Ter
ENST00000636179.1:n.3163C>A
ENST00000636413.1:c.2858C>A	ENSP00000490508.1:p.Ser953Ter
ENST00000636471.1:c.3269C>A	ENSP00000490317.1:p.Ser1090Ter
ENST00000636732.2:c.*2911C>A	ENSP00000490175.1:n.*2911C>A
ENST00000636820.1:n.3294C>A
ENST00000637045.1:c.2858C>A	ENSP00000490141.1:p.Ser953Ter
ENST00000637304.1:c.2858C>A	ENSP00000490872.1:p.Ser953Ter
ENST00000638007.1:c.2858C>A	ENSP00000490723.1:p.Ser953Ter
ENST00000638087.1:c.2858C>A	ENSP00000490673.1:p.Ser953Ter
ENST00000638128.1:c.2417C>A	ENSP00000490934.1:p.Ser806Ter
ENST00000639389.1:c.151+6510C>A	ENSP00000492572.1:n.151+6510C>A
ENST00000647488.1:c.414C>A	ENSP00000494820.1:n.414C>A
ENST00000675069.1:c.725C>A	ENSP00000502467.1:p.Ser242Ter
ENST00000303660.8:c.3191C>A	ENSP00000302501.4:p.Ser1064Ter
ENST00000409487.7:c.3194C>A	ENSP00000386854.2:p.Ser1065Ter
ENST00000419938.5:c.656-1020C>A	ENSP00000394777.2:n.656-1020C>A
ENST00000539609.7:c.3122C>A	ENSP00000443792.2:p.Ser1041Ter
ENST00000558170.6:c.3194C>A	ENSP00000454157.1:p.Ser1065Ter
ENST00000627532.2:c.3194C>A	ENSP00000487174.1:p.Ser1065Ter
NM_001171653.1:c.3122C>A	NP_001165124.1:p.Ser1041Ter
NM_014795.3:c.3194C>A	NP_055610.1:p.Ser1065Ter
XM_006712881.2:c.3194C>A	XP_006712944.1:p.Ser1065Ter
XM_006712882.2:c.3194C>A	XP_006712945.1:p.Ser1065Ter
XM_011512231.1:c.3185C>A	XP_011510533.1:p.Ser1062Ter
XM_011512232.1:c.3173C>A	XP_011510534.1:p.Ser1058Ter
NM_014795.4:c.3194C>A MANE Select	NP_055610.1:p.Ser1065Ter
NM_001171653.2:c.3122C>A	NP_001165124.1:p.Ser1041Ter