Canonical Allele Identifier: CA429441180
Gene: ZEB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.145147309A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389742A>C , CM000664.2:g.144389742A>C GRCh38
NC_000002.11:g.145147309A>C , CM000664.1:g.145147309A>C GRCh37
NC_000002.10:g.144863779A>C NCBI36
NG_016431.1:g.135650T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3203T>G ENSP00000508434.1:n.*3203T>G
ENST00000440875.6:c.2577T>G ENSP00000475553.3:p.Pro859=
ENST00000627532.3:c.3354T>G MANE Select ENSP00000487174.1:p.Pro1118=
ENST00000636026.2:c.3242T>G ENSP00000490776.1:p.Leu1081Arg
ENST00000636179.1:n.3323T>G
ENST00000636413.1:c.3018T>G ENSP00000490508.1:p.Pro1006=
ENST00000636471.1:c.3429T>G ENSP00000490317.1:p.Pro1143=
ENST00000636732.2:c.*3071T>G ENSP00000490175.1:n.*3071T>G
ENST00000636820.1:n.3454T>G
ENST00000637045.1:c.3018T>G ENSP00000490141.1:p.Pro1006=
ENST00000637304.1:c.3018T>G ENSP00000490872.1:p.Pro1006=
ENST00000638007.1:c.3018T>G ENSP00000490723.1:p.Pro1006=
ENST00000638087.1:c.3018T>G ENSP00000490673.1:p.Pro1006=
ENST00000638128.1:c.2577T>G ENSP00000490934.1:p.Pro859=
ENST00000639389.1:c.151+6670T>G ENSP00000492572.1:n.151+6670T>G
ENST00000647488.1:c.574T>G ENSP00000494820.1:n.574T>G
ENST00000675069.1:c.885T>G ENSP00000502467.1:p.Pro295=
ENST00000303660.8:c.3351T>G ENSP00000302501.4:p.Pro1117=
ENST00000409487.7:c.3354T>G ENSP00000386854.2:p.Pro1118=
ENST00000419938.5:c.656-860T>G ENSP00000394777.2:n.656-860T>G
ENST00000539609.7:c.3282T>G ENSP00000443792.2:p.Pro1094=
ENST00000558170.6:c.3354T>G ENSP00000454157.1:p.Pro1118=
ENST00000627532.2:c.3354T>G ENSP00000487174.1:p.Pro1118=
NM_001171653.1:c.3282T>G NP_001165124.1:p.Pro1094=
NM_014795.3:c.3354T>G NP_055610.1:p.Pro1118=
XM_006712881.2:c.3354T>G XP_006712944.1:p.Pro1118=
XM_006712882.2:c.3354T>G XP_006712945.1:p.Pro1118=
XM_011512231.1:c.3345T>G XP_011510533.1:p.Pro1115=
XM_011512232.1:c.3333T>G XP_011510534.1:p.Pro1111=
NM_014795.4:c.3354T>G MANE Select NP_055610.1:p.Pro1118=
NM_001171653.2:c.3282T>G NP_001165124.1:p.Pro1094=