Canonical Allele Identifier: CA348699503

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144389737-C-A
• MyVariant Identifiers: chr2:g.145147304C>A (hg19) ; chr2:g.144389737C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389737C>A , CM000664.2:g.144389737C>A	GRCh38
NC_000002.11:g.145147304C>A , CM000664.1:g.145147304C>A	GRCh37
NC_000002.10:g.144863774C>A	NCBI36
NG_016431.1:g.135655G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3208G>T	ENSP00000508434.1:n.*3208G>T
ENST00000440875.6:c.2582G>T	ENSP00000475553.3:p.Gly861Val
ENST00000627532.3:c.3359G>T MANE Select	ENSP00000487174.1:p.Gly1120Val
ENST00000636026.2:c.3247G>T	ENSP00000490776.1:p.Gly1083Cys
ENST00000636179.1:n.3328G>T
ENST00000636413.1:c.3023G>T	ENSP00000490508.1:p.Gly1008Val
ENST00000636471.1:c.3434G>T	ENSP00000490317.1:p.Gly1145Val
ENST00000636732.2:c.*3076G>T	ENSP00000490175.1:n.*3076G>T
ENST00000636820.1:n.3459G>T
ENST00000637045.1:c.3023G>T	ENSP00000490141.1:p.Gly1008Val
ENST00000637304.1:c.3023G>T	ENSP00000490872.1:p.Gly1008Val
ENST00000638007.1:c.3023G>T	ENSP00000490723.1:p.Gly1008Val
ENST00000638087.1:c.3023G>T	ENSP00000490673.1:p.Gly1008Val
ENST00000638128.1:c.2582G>T	ENSP00000490934.1:p.Gly861Val
ENST00000639389.1:c.151+6675G>T	ENSP00000492572.1:n.151+6675G>T
ENST00000647488.1:c.579G>T	ENSP00000494820.1:n.579G>T
ENST00000675069.1:c.890G>T	ENSP00000502467.1:p.Gly297Val
ENST00000303660.8:c.3356G>T	ENSP00000302501.4:p.Gly1119Val
ENST00000409487.7:c.3359G>T	ENSP00000386854.2:p.Gly1120Val
ENST00000419938.5:c.656-855G>T	ENSP00000394777.2:n.656-855G>T
ENST00000539609.7:c.3287G>T	ENSP00000443792.2:p.Gly1096Val
ENST00000558170.6:c.3359G>T	ENSP00000454157.1:p.Gly1120Val
ENST00000627532.2:c.3359G>T	ENSP00000487174.1:p.Gly1120Val
NM_001171653.1:c.3287G>T	NP_001165124.1:p.Gly1096Val
NM_014795.3:c.3359G>T	NP_055610.1:p.Gly1120Val
XM_006712881.2:c.3359G>T	XP_006712944.1:p.Gly1120Val
XM_006712882.2:c.3359G>T	XP_006712945.1:p.Gly1120Val
XM_011512231.1:c.3350G>T	XP_011510533.1:p.Gly1117Val
XM_011512232.1:c.3338G>T	XP_011510534.1:p.Gly1113Val
NM_014795.4:c.3359G>T MANE Select	NP_055610.1:p.Gly1120Val
NM_001171653.2:c.3287G>T	NP_001165124.1:p.Gly1096Val