Canonical Allele Identifier: CA429445144

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144399249-T-G
• MyVariant Identifiers: chr2:g.145156816T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399249T>G , CM000664.2:g.144399249T>G	GRCh38
NC_000002.11:g.145156816T>G , CM000664.1:g.145156816T>G	GRCh37
NC_000002.10:g.144873286T>G	NCBI36
NG_016431.1:g.126143A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1787A>C	ENSP00000508434.1:n.*1787A>C
ENST00000440875.6:c.1161A>C	ENSP00000475553.3:p.Thr387=
ENST00000627532.3:c.1938A>C MANE Select	ENSP00000487174.1:p.Thr646=
ENST00000636026.2:c.1938A>C	ENSP00000490776.1:p.Thr646=
ENST00000636179.1:n.1907A>C
ENST00000636413.1:c.1602A>C	ENSP00000490508.1:p.Thr534=
ENST00000636471.1:c.2013A>C	ENSP00000490317.1:p.Thr671=
ENST00000636732.2:c.*1655A>C	ENSP00000490175.1:n.*1655A>C
ENST00000636820.1:n.2038A>C
ENST00000637045.1:c.1602A>C	ENSP00000490141.1:p.Thr534=
ENST00000637304.1:c.1602A>C	ENSP00000490872.1:p.Thr534=
ENST00000638007.1:c.1602A>C	ENSP00000490723.1:p.Thr534=
ENST00000638087.1:c.1602A>C	ENSP00000490673.1:p.Thr534=
ENST00000638128.1:c.1161A>C	ENSP00000490934.1:p.Thr387=
ENST00000675069.1:c.-133-399A>C	ENSP00000502467.1:n.-133-399A>C
ENST00000675145.1:n.2486A>C
ENST00000303660.8:c.1935A>C	ENSP00000302501.4:p.Thr645=
ENST00000409487.7:c.1938A>C	ENSP00000386854.2:p.Thr646=
ENST00000419938.5:c.655+1950A>C	ENSP00000394777.2:n.655+1950A>C
ENST00000427902.5:c.2025A>C	ENSP00000395496.2:p.Thr675=
ENST00000440875.5:c.1167+288A>C	ENSP00000475553.2:n.1167+288A>C
ENST00000539609.7:c.1866A>C	ENSP00000443792.2:p.Thr622=
ENST00000558170.6:c.1938A>C	ENSP00000454157.1:p.Thr646=
ENST00000627532.2:c.1938A>C	ENSP00000487174.1:p.Thr646=
NM_001171653.1:c.1866A>C	NP_001165124.1:p.Thr622=
NM_014795.3:c.1938A>C	NP_055610.1:p.Thr646=
XM_006712881.2:c.1938A>C	XP_006712944.1:p.Thr646=
XM_006712882.2:c.1938A>C	XP_006712945.1:p.Thr646=
XM_011512231.1:c.1929A>C	XP_011510533.1:p.Thr643=
XM_011512232.1:c.1917A>C	XP_011510534.1:p.Thr639=
NM_014795.4:c.1938A>C MANE Select	NP_055610.1:p.Thr646=
NM_001171653.2:c.1866A>C	NP_001165124.1:p.Thr622=