Canonical Allele Identifier: CA2790963050

Gene: WT1

Linked Data

• ClinVar Variation Id: 3073651
• ClinVar RCV Id: RCV004016657

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435354A>C , CM000673.2:g.32435354A>C	GRCh38
NC_000011.9:g.32456900A>C , CM000673.1:g.32456900A>C	GRCh37
NC_000011.8:g.32413476A>C	NCBI36
NG_009272.1:g.5188T>G , LRG_525:g.5188T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.7T>G	ENSP00000331327.5:p.Phe3Val
ENST00000379077.9:c.7T>G	ENSP00000368368.5:p.Phe3Val
ENST00000448076.9:c.7T>G	ENSP00000413452.5:p.Phe3Val
ENST00000452863.10:c.7T>G MANE Select	ENSP00000415516.5:p.Phe3Val
ENST00000639563.3:c.7T>G	ENSP00000492269.3:p.Phe3Val
ENST00000332351.7:c.-9T>G	ENSP00000331327.3:n.-9T>G
ENST00000379077.7:c.-9T>G	ENSP00000368368.3:n.-9T>G
ENST00000448076.7:c.-9T>G	ENSP00000413452.3:n.-9T>G
NM_000378.4:c.-9T>G	NP_000369.3:n.-9T>G
NM_024424.3:c.-9T>G	NP_077742.2:n.-9T>G
NM_024426.4:c.-9T>G	NP_077744.3:n.-9T>G
NM_000378.5:c.7T>G	NP_000369.4:p.Phe3Val
NM_024424.4:c.7T>G	NP_077742.3:p.Phe3Val
NM_024426.5:c.7T>G	NP_077744.4:p.Phe3Val
NR_160306.1:n.186T>G
NM_000378.6:c.7T>G	NP_000369.4:p.Phe3Val
NM_024424.5:c.7T>G	NP_077742.3:p.Phe3Val
NM_024426.6:c.7T>G MANE Select	NP_077744.4:p.Phe3Val