Canonical Allele Identifier: CA2661359722

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144390120-AGCGTGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144390122_144390127del , CM000664.2:g.144390122_144390127del	GRCh38
NC_000002.11:g.145147689_145147694del , CM000664.1:g.145147689_145147694del	GRCh37
NC_000002.10:g.144864159_144864164del	NCBI36
NG_016431.1:g.135266_135271del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2917-98_*2917-93del	ENSP00000508434.1:n.*2917-98_*2917-93del
ENST00000440875.6:c.2291-98_2291-93del	ENSP00000475553.3:n.2291-98_2291-93del
ENST00000627532.3:c.3068-98_3068-93del MANE Select	ENSP00000487174.1:n.3068-98_3068-93del
ENST00000636026.2:c.3068-98_3068-93del	ENSP00000490776.1:n.3068-98_3068-93del
ENST00000636179.1:n.3037-98_3037-93del
ENST00000636413.1:c.2732-98_2732-93del	ENSP00000490508.1:n.2732-98_2732-93del
ENST00000636471.1:c.3143-98_3143-93del	ENSP00000490317.1:n.3143-98_3143-93del
ENST00000636732.2:c.*2785-98_*2785-93del	ENSP00000490175.1:n.*2785-98_*2785-93del
ENST00000636820.1:n.3168-98_3168-93del
ENST00000637045.1:c.2732-98_2732-93del	ENSP00000490141.1:n.2732-98_2732-93del
ENST00000637304.1:c.2732-98_2732-93del	ENSP00000490872.1:n.2732-98_2732-93del
ENST00000638007.1:c.2732-98_2732-93del	ENSP00000490723.1:n.2732-98_2732-93del
ENST00000638087.1:c.2732-98_2732-93del	ENSP00000490673.1:n.2732-98_2732-93del
ENST00000638128.1:c.2291-98_2291-93del	ENSP00000490934.1:n.2291-98_2291-93del
ENST00000639389.1:c.151+6286_151+6291del	ENSP00000492572.1:n.151+6286_151+6291del
ENST00000647488.1:c.288-98_288-93del	ENSP00000494820.1:n.288-98_288-93del
ENST00000675069.1:c.599-98_599-93del	ENSP00000502467.1:n.599-98_599-93del
ENST00000303660.8:c.3065-98_3065-93del	ENSP00000302501.4:n.3065-98_3065-93del
ENST00000409487.7:c.3068-98_3068-93del	ENSP00000386854.2:n.3068-98_3068-93del
ENST00000419938.5:c.656-1244_656-1239del	ENSP00000394777.2:n.656-1244_656-1239del
ENST00000539609.7:c.2996-98_2996-93del	ENSP00000443792.2:n.2996-98_2996-93del
ENST00000558170.6:c.3068-98_3068-93del	ENSP00000454157.1:n.3068-98_3068-93del
ENST00000627532.2:c.3068-98_3068-93del	ENSP00000487174.1:n.3068-98_3068-93del
NM_001171653.1:c.2996-98_2996-93del	NP_001165124.1:n.2996-98_2996-93del
NM_014795.3:c.3068-98_3068-93del	NP_055610.1:n.3068-98_3068-93del
XM_006712881.2:c.3068-98_3068-93del	XP_006712944.1:n.3068-98_3068-93del
XM_006712882.2:c.3068-98_3068-93del	XP_006712945.1:n.3068-98_3068-93del
XM_011512231.1:c.3059-98_3059-93del	XP_011510533.1:n.3059-98_3059-93del
XM_011512232.1:c.3047-98_3047-93del	XP_011510534.1:n.3047-98_3047-93del
NM_014795.4:c.3068-98_3068-93del MANE Select	NP_055610.1:n.3068-98_3068-93del
NM_001171653.2:c.2996-98_2996-93del	NP_001165124.1:n.2996-98_2996-93del