Canonical Allele Identifier: CA348708452

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144398825-G-T
• COSMIC: COSM278202
• MyVariant Identifiers: chr2:g.145156392G>T (hg19) ; chr2:g.144398825G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398825G>T , CM000664.2:g.144398825G>T	GRCh38
NC_000002.11:g.145156392G>T , CM000664.1:g.145156392G>T	GRCh37
NC_000002.10:g.144872862G>T	NCBI36
NG_016431.1:g.126567C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2211C>A	ENSP00000508434.1:n.*2211C>A
ENST00000440875.6:c.1585C>A	ENSP00000475553.3:p.Leu529Ile
ENST00000627532.3:c.2362C>A MANE Select	ENSP00000487174.1:p.Leu788Ile
ENST00000636026.2:c.2362C>A	ENSP00000490776.1:p.Leu788Ile
ENST00000636179.1:n.2331C>A
ENST00000636413.1:c.2026C>A	ENSP00000490508.1:p.Leu676Ile
ENST00000636471.1:c.2437C>A	ENSP00000490317.1:p.Leu813Ile
ENST00000636732.2:c.*2079C>A	ENSP00000490175.1:n.*2079C>A
ENST00000636820.1:n.2462C>A
ENST00000637045.1:c.2026C>A	ENSP00000490141.1:p.Leu676Ile
ENST00000637304.1:c.2026C>A	ENSP00000490872.1:p.Leu676Ile
ENST00000638007.1:c.2026C>A	ENSP00000490723.1:p.Leu676Ile
ENST00000638087.1:c.2026C>A	ENSP00000490673.1:p.Leu676Ile
ENST00000638128.1:c.1585C>A	ENSP00000490934.1:p.Leu529Ile
ENST00000675069.1:c.-108C>A	ENSP00000502467.1:n.-108C>A
ENST00000675145.1:n.2910C>A
ENST00000303660.8:c.2359C>A	ENSP00000302501.4:p.Leu787Ile
ENST00000409487.7:c.2362C>A	ENSP00000386854.2:p.Leu788Ile
ENST00000419938.5:c.655+2374C>A	ENSP00000394777.2:n.655+2374C>A
ENST00000440875.5:c.1167+712C>A	ENSP00000475553.2:n.1167+712C>A
ENST00000539609.7:c.2290C>A	ENSP00000443792.2:p.Leu764Ile
ENST00000558170.6:c.2362C>A	ENSP00000454157.1:p.Leu788Ile
ENST00000627532.2:c.2362C>A	ENSP00000487174.1:p.Leu788Ile
NM_001171653.1:c.2290C>A	NP_001165124.1:p.Leu764Ile
NM_014795.3:c.2362C>A	NP_055610.1:p.Leu788Ile
XM_006712881.2:c.2362C>A	XP_006712944.1:p.Leu788Ile
XM_006712882.2:c.2362C>A	XP_006712945.1:p.Leu788Ile
XM_011512231.1:c.2353C>A	XP_011510533.1:p.Leu785Ile
XM_011512232.1:c.2341C>A	XP_011510534.1:p.Leu781Ile
NM_014795.4:c.2362C>A MANE Select	NP_055610.1:p.Leu788Ile
NM_001171653.2:c.2290C>A	NP_001165124.1:p.Leu764Ile