Canonical Allele Identifier: CA429217651

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145154139T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396572T>G , CM000664.2:g.144396572T>G	GRCh38
NC_000002.11:g.145154139T>G , CM000664.1:g.145154139T>G	GRCh37
NC_000002.10:g.144870609T>G	NCBI36
NG_016431.1:g.128820A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2756A>C	ENSP00000508434.1:n.*2756A>C
ENST00000440875.6:c.2130A>C	ENSP00000475553.3:p.Ala710=
ENST00000627532.3:c.2907A>C MANE Select	ENSP00000487174.1:p.Ala969=
ENST00000636026.2:c.2907A>C	ENSP00000490776.1:p.Ala969=
ENST00000636179.1:n.2876A>C
ENST00000636413.1:c.2571A>C	ENSP00000490508.1:p.Ala857=
ENST00000636471.1:c.2982A>C	ENSP00000490317.1:p.Ala994=
ENST00000636732.2:c.*2624A>C	ENSP00000490175.1:n.*2624A>C
ENST00000636820.1:n.3007A>C
ENST00000637045.1:c.2571A>C	ENSP00000490141.1:p.Ala857=
ENST00000637304.1:c.2571A>C	ENSP00000490872.1:p.Ala857=
ENST00000638007.1:c.2571A>C	ENSP00000490723.1:p.Ala857=
ENST00000638087.1:c.2571A>C	ENSP00000490673.1:p.Ala857=
ENST00000638128.1:c.2130A>C	ENSP00000490934.1:p.Ala710=
ENST00000647488.1:c.39A>C	ENSP00000494820.1:p.Ala13=
ENST00000675069.1:c.438A>C	ENSP00000502467.1:p.Ala146=
ENST00000303660.8:c.2904A>C	ENSP00000302501.4:p.Ala968=
ENST00000409487.7:c.2907A>C	ENSP00000386854.2:p.Ala969=
ENST00000419938.5:c.655+4627A>C	ENSP00000394777.2:n.655+4627A>C
ENST00000539609.7:c.2835A>C	ENSP00000443792.2:p.Ala945=
ENST00000558170.6:c.2907A>C	ENSP00000454157.1:p.Ala969=
ENST00000627532.2:c.2907A>C	ENSP00000487174.1:p.Ala969=
NM_001171653.1:c.2835A>C	NP_001165124.1:p.Ala945=
NM_014795.3:c.2907A>C	NP_055610.1:p.Ala969=
XM_006712881.2:c.2907A>C	XP_006712944.1:p.Ala969=
XM_006712882.2:c.2907A>C	XP_006712945.1:p.Ala969=
XM_011512231.1:c.2898A>C	XP_011510533.1:p.Ala966=
XM_011512232.1:c.2886A>C	XP_011510534.1:p.Ala962=
NM_014795.4:c.2907A>C MANE Select	NP_055610.1:p.Ala969=
NM_001171653.2:c.2835A>C	NP_001165124.1:p.Ala945=