Canonical Allele Identifier: CA348708499

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144398846-T-C
• MyVariant Identifiers: chr2:g.145156413T>C (hg19) ; chr2:g.144398846T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398846T>C , CM000664.2:g.144398846T>C	GRCh38
NC_000002.11:g.145156413T>C , CM000664.1:g.145156413T>C	GRCh37
NC_000002.10:g.144872883T>C	NCBI36
NG_016431.1:g.126546A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2190A>G	ENSP00000508434.1:n.*2190A>G
ENST00000440875.6:c.1564A>G	ENSP00000475553.3:p.Asn522Asp
ENST00000627532.3:c.2341A>G MANE Select	ENSP00000487174.1:p.Asn781Asp
ENST00000636026.2:c.2341A>G	ENSP00000490776.1:p.Asn781Asp
ENST00000636179.1:n.2310A>G
ENST00000636413.1:c.2005A>G	ENSP00000490508.1:p.Asn669Asp
ENST00000636471.1:c.2416A>G	ENSP00000490317.1:p.Asn806Asp
ENST00000636732.2:c.*2058A>G	ENSP00000490175.1:n.*2058A>G
ENST00000636820.1:n.2441A>G
ENST00000637045.1:c.2005A>G	ENSP00000490141.1:p.Asn669Asp
ENST00000637304.1:c.2005A>G	ENSP00000490872.1:p.Asn669Asp
ENST00000638007.1:c.2005A>G	ENSP00000490723.1:p.Asn669Asp
ENST00000638087.1:c.2005A>G	ENSP00000490673.1:p.Asn669Asp
ENST00000638128.1:c.1564A>G	ENSP00000490934.1:p.Asn522Asp
ENST00000675069.1:c.-129A>G	ENSP00000502467.1:n.-129A>G
ENST00000675145.1:n.2889A>G
ENST00000303660.8:c.2338A>G	ENSP00000302501.4:p.Asn780Asp
ENST00000409487.7:c.2341A>G	ENSP00000386854.2:p.Asn781Asp
ENST00000419938.5:c.655+2353A>G	ENSP00000394777.2:n.655+2353A>G
ENST00000440875.5:c.1167+691A>G	ENSP00000475553.2:n.1167+691A>G
ENST00000539609.7:c.2269A>G	ENSP00000443792.2:p.Asn757Asp
ENST00000558170.6:c.2341A>G	ENSP00000454157.1:p.Asn781Asp
ENST00000627532.2:c.2341A>G	ENSP00000487174.1:p.Asn781Asp
NM_001171653.1:c.2269A>G	NP_001165124.1:p.Asn757Asp
NM_014795.3:c.2341A>G	NP_055610.1:p.Asn781Asp
XM_006712881.2:c.2341A>G	XP_006712944.1:p.Asn781Asp
XM_006712882.2:c.2341A>G	XP_006712945.1:p.Asn781Asp
XM_011512231.1:c.2332A>G	XP_011510533.1:p.Asn778Asp
XM_011512232.1:c.2320A>G	XP_011510534.1:p.Asn774Asp
NM_014795.4:c.2341A>G MANE Select	NP_055610.1:p.Asn781Asp
NM_001171653.2:c.2269A>G	NP_001165124.1:p.Asn757Asp