Canonical Allele Identifier: CA379963267

Gene: WT1

Linked Data

• ClinVar Variation Id: 1444084
• ClinVar RCV Id: RCV001981634
• dbSNP Id: rs1311184469
• gnomAD v2: 11-32450051-C-T
• gnomAD v4: 11-32428505-C-T
• MyVariant Identifiers: chr11:g.32450051C>T (hg19) ; chr11:g.32428505C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428505C>T , CM000673.2:g.32428505C>T	GRCh38
NC_000011.9:g.32450051C>T , CM000673.1:g.32450051C>T	GRCh37
NC_000011.8:g.32406627C>T	NCBI36
NG_009272.1:g.12037G>A , LRG_525:g.12037G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.776G>A	ENSP00000331327.5:p.Gly259Asp
ENST00000379077.9:c.776G>A	ENSP00000368368.5:p.Gly259Asp
ENST00000379079.8:c.125G>A	ENSP00000368370.2:p.Gly42Asp
ENST00000448076.9:c.776G>A	ENSP00000413452.5:p.Gly259Asp
ENST00000452863.10:c.776G>A MANE Select	ENSP00000415516.5:p.Gly259Asp
ENST00000639563.3:c.776G>A	ENSP00000492269.3:p.Gly259Asp
ENST00000640146.2:c.152G>A	ENSP00000491984.2:p.Gly51Asp
ENST00000332351.7:c.761G>A	ENSP00000331327.3:p.Gly254Asp
ENST00000379077.7:c.761G>A	ENSP00000368368.3:p.Gly254Asp
ENST00000379079.6:c.125G>A	ENSP00000368370.2:p.Gly42Asp
ENST00000448076.7:c.761G>A	ENSP00000413452.3:p.Gly254Asp
ENST00000452863.7:c.761G>A	ENSP00000415516.3:p.Gly254Asp
ENST00000527775.1:c.14G>A	ENSP00000435351.1:p.Gly5Asp
ENST00000530998.5:c.125G>A	ENSP00000435307.1:p.Gly42Asp
NM_000378.4:c.761G>A	NP_000369.3:p.Gly254Asp
NM_001198551.1:c.125G>A , LRG_525t2:c.125G>A	NP_001185480.1:p.Gly42Asp
NM_001198552.1:c.125G>A	NP_001185481.1:p.Gly42Asp
NM_024424.3:c.761G>A	NP_077742.2:p.Gly254Asp
NM_024426.4:c.761G>A	NP_077744.3:p.Gly254Asp
NM_000378.5:c.776G>A	NP_000369.4:p.Gly259Asp
NM_024424.4:c.776G>A	NP_077742.3:p.Gly259Asp
NM_024426.5:c.776G>A	NP_077744.4:p.Gly259Asp
NR_160306.1:n.955G>A
NM_000378.6:c.776G>A	NP_000369.4:p.Gly259Asp
NM_001198552.2:c.125G>A	NP_001185481.1:p.Gly42Asp
NM_024424.5:c.776G>A	NP_077742.3:p.Gly259Asp
NM_024426.6:c.776G>A MANE Select	NP_077744.4:p.Gly259Asp