Canonical Allele Identifier: CA2661359653

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144389357-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389357G>A , CM000664.2:g.144389357G>A	GRCh38
NC_000002.11:g.145146924G>A , CM000664.1:g.145146924G>A	GRCh37
NC_000002.10:g.144863394G>A	NCBI36
NG_016431.1:g.136035C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3588C>T	ENSP00000508434.1:n.*3588C>T
ENST00000440875.6:c.*94C>T	ENSP00000475553.3:n.*94C>T
ENST00000627532.3:c.*94C>T MANE Select	ENSP00000487174.1:n.*94C>T
ENST00000636026.2:c.*18C>T	ENSP00000490776.1:n.*18C>T
ENST00000636179.1:n.3708C>T
ENST00000636413.1:c.*94C>T	ENSP00000490508.1:n.*94C>T
ENST00000636471.1:c.*94C>T	ENSP00000490317.1:n.*94C>T
ENST00000636732.2:c.*3456C>T	ENSP00000490175.1:n.*3456C>T
ENST00000636820.1:n.3839C>T
ENST00000637045.1:c.*94C>T	ENSP00000490141.1:n.*94C>T
ENST00000637304.1:c.*94C>T	ENSP00000490872.1:n.*94C>T
ENST00000638007.1:c.*94C>T	ENSP00000490723.1:n.*94C>T
ENST00000638087.1:c.*94C>T	ENSP00000490673.1:n.*94C>T
ENST00000638128.1:c.*94C>T	ENSP00000490934.1:n.*94C>T
ENST00000639389.1:c.151+7055C>T	ENSP00000492572.1:n.151+7055C>T
ENST00000647488.1:c.959C>T	ENSP00000494820.1:n.959C>T
ENST00000675069.1:c.*94C>T	ENSP00000502467.1:n.*94C>T
ENST00000303660.8:c.*94C>T	ENSP00000302501.4:n.*94C>T
ENST00000409487.7:c.*94C>T	ENSP00000386854.2:n.*94C>T
ENST00000419938.5:c.656-475C>T	ENSP00000394777.2:n.656-475C>T
ENST00000539609.7:c.*94C>T	ENSP00000443792.2:n.*94C>T
ENST00000558170.6:c.*94C>T	ENSP00000454157.1:n.*94C>T
ENST00000627532.2:c.*94C>T	ENSP00000487174.1:n.*94C>T
NM_001171653.1:c.*94C>T	NP_001165124.1:n.*94C>T
NM_014795.3:c.*94C>T	NP_055610.1:n.*94C>T
XM_006712881.2:c.*94C>T	XP_006712944.1:n.*94C>T
XM_006712882.2:c.*94C>T	XP_006712945.1:n.*94C>T
XM_011512231.1:c.*94C>T	XP_011510533.1:n.*94C>T
XM_011512232.1:c.*94C>T	XP_011510534.1:n.*94C>T
NM_014795.4:c.*94C>T MANE Select	NP_055610.1:n.*94C>T
NM_001171653.2:c.*94C>T	NP_001165124.1:n.*94C>T