Canonical Allele Identifier: CA429217591

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144396472-A-G
• MyVariant Identifiers: chr2:g.145154039A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396472A>G , CM000664.2:g.144396472A>G	GRCh38
NC_000002.11:g.145154039A>G , CM000664.1:g.145154039A>G	GRCh37
NC_000002.10:g.144870509A>G	NCBI36
NG_016431.1:g.128920T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2856T>C	ENSP00000508434.1:n.*2856T>C
ENST00000440875.6:c.2230T>C	ENSP00000475553.3:p.Leu744=
ENST00000627532.3:c.3007T>C MANE Select	ENSP00000487174.1:p.Leu1003=
ENST00000636026.2:c.3007T>C	ENSP00000490776.1:p.Leu1003=
ENST00000636179.1:n.2976T>C
ENST00000636413.1:c.2671T>C	ENSP00000490508.1:p.Leu891=
ENST00000636471.1:c.3082T>C	ENSP00000490317.1:p.Leu1028=
ENST00000636732.2:c.*2724T>C	ENSP00000490175.1:n.*2724T>C
ENST00000636820.1:n.3107T>C
ENST00000637045.1:c.2671T>C	ENSP00000490141.1:p.Leu891=
ENST00000637304.1:c.2671T>C	ENSP00000490872.1:p.Leu891=
ENST00000638007.1:c.2671T>C	ENSP00000490723.1:p.Leu891=
ENST00000638087.1:c.2671T>C	ENSP00000490673.1:p.Leu891=
ENST00000638128.1:c.2230T>C	ENSP00000490934.1:p.Leu744=
ENST00000639389.1:c.91T>C	ENSP00000492572.1:p.Leu31=
ENST00000647488.1:c.139T>C	ENSP00000494820.1:p.Leu47=
ENST00000675069.1:c.538T>C	ENSP00000502467.1:p.Leu180=
ENST00000303660.8:c.3004T>C	ENSP00000302501.4:p.Leu1002=
ENST00000409487.7:c.3007T>C	ENSP00000386854.2:p.Leu1003=
ENST00000419938.5:c.655+4727T>C	ENSP00000394777.2:n.655+4727T>C
ENST00000539609.7:c.2935T>C	ENSP00000443792.2:p.Leu979=
ENST00000558170.6:c.3007T>C	ENSP00000454157.1:p.Leu1003=
ENST00000627532.2:c.3007T>C	ENSP00000487174.1:p.Leu1003=
NM_001171653.1:c.2935T>C	NP_001165124.1:p.Leu979=
NM_014795.3:c.3007T>C	NP_055610.1:p.Leu1003=
XM_006712881.2:c.3007T>C	XP_006712944.1:p.Leu1003=
XM_006712882.2:c.3007T>C	XP_006712945.1:p.Leu1003=
XM_011512231.1:c.2998T>C	XP_011510533.1:p.Leu1000=
XM_011512232.1:c.2986T>C	XP_011510534.1:p.Leu996=
NM_014795.4:c.3007T>C MANE Select	NP_055610.1:p.Leu1003=
NM_001171653.2:c.2935T>C	NP_001165124.1:p.Leu979=