Canonical Allele Identifier: CA348708526

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156424T>G (hg19) ; chr2:g.144398857T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398857T>G , CM000664.2:g.144398857T>G	GRCh38
NC_000002.11:g.145156424T>G , CM000664.1:g.145156424T>G	GRCh37
NC_000002.10:g.144872894T>G	NCBI36
NG_016431.1:g.126535A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2179A>C	ENSP00000508434.1:n.*2179A>C
ENST00000440875.6:c.1553A>C	ENSP00000475553.3:p.His518Pro
ENST00000627532.3:c.2330A>C MANE Select	ENSP00000487174.1:p.His777Pro
ENST00000636026.2:c.2330A>C	ENSP00000490776.1:p.His777Pro
ENST00000636179.1:n.2299A>C
ENST00000636413.1:c.1994A>C	ENSP00000490508.1:p.His665Pro
ENST00000636471.1:c.2405A>C	ENSP00000490317.1:p.His802Pro
ENST00000636732.2:c.*2047A>C	ENSP00000490175.1:n.*2047A>C
ENST00000636820.1:n.2430A>C
ENST00000637045.1:c.1994A>C	ENSP00000490141.1:p.His665Pro
ENST00000637304.1:c.1994A>C	ENSP00000490872.1:p.His665Pro
ENST00000638007.1:c.1994A>C	ENSP00000490723.1:p.His665Pro
ENST00000638087.1:c.1994A>C	ENSP00000490673.1:p.His665Pro
ENST00000638128.1:c.1553A>C	ENSP00000490934.1:p.His518Pro
ENST00000675069.1:c.-133-7A>C	ENSP00000502467.1:n.-133-7A>C
ENST00000675145.1:n.2878A>C
ENST00000303660.8:c.2327A>C	ENSP00000302501.4:p.His776Pro
ENST00000409487.7:c.2330A>C	ENSP00000386854.2:p.His777Pro
ENST00000419938.5:c.655+2342A>C	ENSP00000394777.2:n.655+2342A>C
ENST00000440875.5:c.1167+680A>C	ENSP00000475553.2:n.1167+680A>C
ENST00000539609.7:c.2258A>C	ENSP00000443792.2:p.His753Pro
ENST00000558170.6:c.2330A>C	ENSP00000454157.1:p.His777Pro
ENST00000627532.2:c.2330A>C	ENSP00000487174.1:p.His777Pro
NM_001171653.1:c.2258A>C	NP_001165124.1:p.His753Pro
NM_014795.3:c.2330A>C	NP_055610.1:p.His777Pro
XM_006712881.2:c.2330A>C	XP_006712944.1:p.His777Pro
XM_006712882.2:c.2330A>C	XP_006712945.1:p.His777Pro
XM_011512231.1:c.2321A>C	XP_011510533.1:p.His774Pro
XM_011512232.1:c.2309A>C	XP_011510534.1:p.His770Pro
NM_014795.4:c.2330A>C MANE Select	NP_055610.1:p.His777Pro
NM_001171653.2:c.2258A>C	NP_001165124.1:p.His753Pro