Canonical Allele Identifier: CA348698938

Gene: ZEB2

Linked Data

• COSMIC: COSM3567342
• MyVariant Identifiers: chr2:g.145147101G>A (hg19) ; chr2:g.144389534G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389534G>A , CM000664.2:g.144389534G>A	GRCh38
NC_000002.11:g.145147101G>A , CM000664.1:g.145147101G>A	GRCh37
NC_000002.10:g.144863571G>A	NCBI36
NG_016431.1:g.135858C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3411C>T	ENSP00000508434.1:n.*3411C>T
ENST00000440875.6:c.2785C>T	ENSP00000475553.3:p.His929Tyr
ENST00000627532.3:c.3562C>T MANE Select	ENSP00000487174.1:p.His1188Tyr
ENST00000636026.2:c.3450C>T	ENSP00000490776.1:p.Ile1150=
ENST00000636179.1:n.3531C>T
ENST00000636413.1:c.3226C>T	ENSP00000490508.1:p.His1076Tyr
ENST00000636471.1:c.3637C>T	ENSP00000490317.1:p.His1213Tyr
ENST00000636732.2:c.*3279C>T	ENSP00000490175.1:n.*3279C>T
ENST00000636820.1:n.3662C>T
ENST00000637045.1:c.3226C>T	ENSP00000490141.1:p.His1076Tyr
ENST00000637304.1:c.3226C>T	ENSP00000490872.1:p.His1076Tyr
ENST00000638007.1:c.3226C>T	ENSP00000490723.1:p.His1076Tyr
ENST00000638087.1:c.3226C>T	ENSP00000490673.1:p.His1076Tyr
ENST00000638128.1:c.2785C>T	ENSP00000490934.1:p.His929Tyr
ENST00000639389.1:c.151+6878C>T	ENSP00000492572.1:n.151+6878C>T
ENST00000647488.1:c.782C>T	ENSP00000494820.1:n.782C>T
ENST00000675069.1:c.1093C>T	ENSP00000502467.1:p.His365Tyr
ENST00000303660.8:c.3559C>T	ENSP00000302501.4:p.His1187Tyr
ENST00000409487.7:c.3562C>T	ENSP00000386854.2:p.His1188Tyr
ENST00000419938.5:c.656-652C>T	ENSP00000394777.2:n.656-652C>T
ENST00000539609.7:c.3490C>T	ENSP00000443792.2:p.His1164Tyr
ENST00000558170.6:c.3562C>T	ENSP00000454157.1:p.His1188Tyr
ENST00000627532.2:c.3562C>T	ENSP00000487174.1:p.His1188Tyr
NM_001171653.1:c.3490C>T	NP_001165124.1:p.His1164Tyr
NM_014795.3:c.3562C>T	NP_055610.1:p.His1188Tyr
XM_006712881.2:c.3562C>T	XP_006712944.1:p.His1188Tyr
XM_006712882.2:c.3562C>T	XP_006712945.1:p.His1188Tyr
XM_011512231.1:c.3553C>T	XP_011510533.1:p.His1185Tyr
XM_011512232.1:c.3541C>T	XP_011510534.1:p.His1181Tyr
NM_014795.4:c.3562C>T MANE Select	NP_055610.1:p.His1188Tyr
NM_001171653.2:c.3490C>T	NP_001165124.1:p.His1164Tyr