Canonical Allele Identifier: CA348706844

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144398381-C-G
• MyVariant Identifiers: chr2:g.145155948C>G (hg19) ; chr2:g.144398381C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398381C>G , CM000664.2:g.144398381C>G	GRCh38
NC_000002.11:g.145155948C>G , CM000664.1:g.145155948C>G	GRCh37
NC_000002.10:g.144872418C>G	NCBI36
NG_016431.1:g.127011G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2655G>C	ENSP00000508434.1:n.*2655G>C
ENST00000440875.6:c.2029G>C	ENSP00000475553.3:p.Ala677Pro
ENST00000627532.3:c.2806G>C MANE Select	ENSP00000487174.1:p.Ala936Pro
ENST00000636026.2:c.2806G>C	ENSP00000490776.1:p.Ala936Pro
ENST00000636179.1:n.2775G>C
ENST00000636413.1:c.2470G>C	ENSP00000490508.1:p.Ala824Pro
ENST00000636471.1:c.2881G>C	ENSP00000490317.1:p.Ala961Pro
ENST00000636732.2:c.*2523G>C	ENSP00000490175.1:n.*2523G>C
ENST00000636820.1:n.2906G>C
ENST00000637045.1:c.2470G>C	ENSP00000490141.1:p.Ala824Pro
ENST00000637304.1:c.2470G>C	ENSP00000490872.1:p.Ala824Pro
ENST00000638007.1:c.2470G>C	ENSP00000490723.1:p.Ala824Pro
ENST00000638087.1:c.2470G>C	ENSP00000490673.1:p.Ala824Pro
ENST00000638128.1:c.2029G>C	ENSP00000490934.1:p.Ala677Pro
ENST00000675069.1:c.337G>C	ENSP00000502467.1:p.Ala113Pro
ENST00000303660.8:c.2803G>C	ENSP00000302501.4:p.Ala935Pro
ENST00000409487.7:c.2806G>C	ENSP00000386854.2:p.Ala936Pro
ENST00000419938.5:c.655+2818G>C	ENSP00000394777.2:n.655+2818G>C
ENST00000440875.5:c.1168-453G>C	ENSP00000475553.2:n.1168-453G>C
ENST00000539609.7:c.2734G>C	ENSP00000443792.2:p.Ala912Pro
ENST00000558170.6:c.2806G>C	ENSP00000454157.1:p.Ala936Pro
ENST00000627532.2:c.2806G>C	ENSP00000487174.1:p.Ala936Pro
NM_001171653.1:c.2734G>C	NP_001165124.1:p.Ala912Pro
NM_014795.3:c.2806G>C	NP_055610.1:p.Ala936Pro
XM_006712881.2:c.2806G>C	XP_006712944.1:p.Ala936Pro
XM_006712882.2:c.2806G>C	XP_006712945.1:p.Ala936Pro
XM_011512231.1:c.2797G>C	XP_011510533.1:p.Ala933Pro
XM_011512232.1:c.2785G>C	XP_011510534.1:p.Ala929Pro
NM_014795.4:c.2806G>C MANE Select	NP_055610.1:p.Ala936Pro
NM_001171653.2:c.2734G>C	NP_001165124.1:p.Ala912Pro