Canonical Allele Identifier: CA348699107
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389579C>A , CM000664.2:g.144389579C>A GRCh38
NC_000002.11:g.145147146C>A , CM000664.1:g.145147146C>A GRCh37
NC_000002.10:g.144863616C>A NCBI36
NG_016431.1:g.135813G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3366G>T ENSP00000508434.1:n.*3366G>T
ENST00000440875.6:c.2740G>T ENSP00000475553.3:p.Asp914Tyr
ENST00000627532.3:c.3517G>T MANE Select ENSP00000487174.1:p.Asp1173Tyr
ENST00000636026.2:c.3405G>T ENSP00000490776.1:p.Trp1135Cys
ENST00000636179.1:n.3486G>T
ENST00000636413.1:c.3181G>T ENSP00000490508.1:p.Asp1061Tyr
ENST00000636471.1:c.3592G>T ENSP00000490317.1:p.Asp1198Tyr
ENST00000636732.2:c.*3234G>T ENSP00000490175.1:n.*3234G>T
ENST00000636820.1:n.3617G>T
ENST00000637045.1:c.3181G>T ENSP00000490141.1:p.Asp1061Tyr
ENST00000637304.1:c.3181G>T ENSP00000490872.1:p.Asp1061Tyr
ENST00000638007.1:c.3181G>T ENSP00000490723.1:p.Asp1061Tyr
ENST00000638087.1:c.3181G>T ENSP00000490673.1:p.Asp1061Tyr
ENST00000638128.1:c.2740G>T ENSP00000490934.1:p.Asp914Tyr
ENST00000639389.1:c.151+6833G>T ENSP00000492572.1:n.151+6833G>T
ENST00000647488.1:c.737G>T ENSP00000494820.1:n.737G>T
ENST00000675069.1:c.1048G>T ENSP00000502467.1:p.Asp350Tyr
ENST00000303660.8:c.3514G>T ENSP00000302501.4:p.Asp1172Tyr
ENST00000409487.7:c.3517G>T ENSP00000386854.2:p.Asp1173Tyr
ENST00000419938.5:c.656-697G>T ENSP00000394777.2:n.656-697G>T
ENST00000539609.7:c.3445G>T ENSP00000443792.2:p.Asp1149Tyr
ENST00000558170.6:c.3517G>T ENSP00000454157.1:p.Asp1173Tyr
ENST00000627532.2:c.3517G>T ENSP00000487174.1:p.Asp1173Tyr
NM_001171653.1:c.3445G>T NP_001165124.1:p.Asp1149Tyr
NM_014795.3:c.3517G>T NP_055610.1:p.Asp1173Tyr
XM_006712881.2:c.3517G>T XP_006712944.1:p.Asp1173Tyr
XM_006712882.2:c.3517G>T XP_006712945.1:p.Asp1173Tyr
XM_011512231.1:c.3508G>T XP_011510533.1:p.Asp1170Tyr
XM_011512232.1:c.3496G>T XP_011510534.1:p.Asp1166Tyr
NM_014795.4:c.3517G>T MANE Select NP_055610.1:p.Asp1173Tyr
NM_001171653.2:c.3445G>T NP_001165124.1:p.Asp1149Tyr