Canonical Allele Identifier: CA3085915256
Community Standard Title: NM_014795.4(ZEB2):c.3095G= (p.Cys1032=)
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144390001C= , CM000664.2:g.144390001C= GRCh38
NC_000002.11:g.145147568C= , CM000664.1:g.145147568C= GRCh37
NC_000002.10:g.144864038C= NCBI36
NG_016431.1:g.135391G=

Transcript Alleles

HGVS Amino-acid Change
NM_014795.4:c.3095G= MANE Select NP_055610.1:p.Cys1032=
ENST00000627532.3:c.3095G= MANE Select ENSP00000487174.1:p.Cys1032=
NM_001171653.1:c.3023G= NP_001165124.1:p.Cys1008=
NM_001171653.2:c.3023G= NP_001165124.1:p.Cys1008=
NM_014795.3:c.3095G= NP_055610.1:p.Cys1032=
ENST00000303660.8:c.3092G= ENSP00000302501.4:p.Cys1031=
ENST00000409487.7:c.3095G= ENSP00000386854.2:p.Cys1032=
ENST00000419938.5:c.656-1119G= ENSP00000394777.2:n.656-1119G=
ENST00000440875.6:c.2318G= ENSP00000475553.3:p.Cys773=
ENST00000539609.7:c.3023G= ENSP00000443792.2:p.Cys1008=
ENST00000558170.6:c.3095G= ENSP00000454157.1:p.Cys1032=
ENST00000627532.2:c.3095G= ENSP00000487174.1:p.Cys1032=
ENST00000636026.2:c.3095G= ENSP00000490776.1:p.Cys1032=
ENST00000636179.1:n.3064G=
ENST00000636413.1:c.2759G= ENSP00000490508.1:p.Cys920=
ENST00000636471.1:c.3170G= ENSP00000490317.1:p.Cys1057=
ENST00000636732.2:c.*2812G= ENSP00000490175.1:n.*2812G=
ENST00000636820.1:n.3195G=
ENST00000637045.1:c.2759G= ENSP00000490141.1:p.Cys920=
ENST00000637304.1:c.2759G= ENSP00000490872.1:p.Cys920=
ENST00000638007.1:c.2759G= ENSP00000490723.1:p.Cys920=
ENST00000638087.1:c.2759G= ENSP00000490673.1:p.Cys920=
ENST00000638128.1:c.2318G= ENSP00000490934.1:p.Cys773=
ENST00000639389.1:c.151+6411G= ENSP00000492572.1:n.151+6411G=
ENST00000647488.1:c.315G= ENSP00000494820.1:n.315G=
ENST00000675069.1:c.626G= ENSP00000502467.1:p.Cys209=
ENST00000689298.1:c.*2944G= ENSP00000508434.1:n.*2944G=
XM_006712881.2:c.3095G= XP_006712944.1:p.Cys1032=
XM_006712882.2:c.3095G= XP_006712945.1:p.Cys1032=
XM_011512231.1:c.3086G= XP_011510533.1:p.Cys1029=
XM_011512232.1:c.3074G= XP_011510534.1:p.Cys1025=