Canonical Allele Identifier: CA379962044
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 620630
ClinVar RCV Id: RCV000761158
dbSNP Id: rs1564987636

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32417592C>T , CM000673.2:g.32417592C>T GRCh38
NC_000011.9:g.32439138C>T , CM000673.1:g.32439138C>T GRCh37
NC_000011.8:g.32395714C>T NCBI36
NG_009272.1:g.22950G>A , LRG_525:g.22950G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.950G>A ENSP00000331327.5:p.Gly317Glu
ENST00000379077.9:c.950G>A ENSP00000368368.5:p.Gly317Glu
ENST00000379079.8:c.299G>A ENSP00000368370.2:p.Gly100Glu
ENST00000448076.9:c.950G>A ENSP00000413452.5:p.Gly317Glu
ENST00000452863.10:c.950G>A MANE Select ENSP00000415516.5:p.Gly317Glu
ENST00000639563.3:c.950G>A ENSP00000492269.3:p.Gly317Glu
ENST00000640146.2:c.326G>A ENSP00000491984.2:p.Gly109Glu
ENST00000332351.7:c.935G>A ENSP00000331327.3:p.Gly312Glu
ENST00000379077.7:c.935G>A ENSP00000368368.3:p.Gly312Glu
ENST00000379079.6:c.299G>A ENSP00000368370.2:p.Gly100Glu
ENST00000448076.7:c.935G>A ENSP00000413452.3:p.Gly312Glu
ENST00000452863.7:c.935G>A ENSP00000415516.3:p.Gly312Glu
ENST00000527775.1:c.188G>A ENSP00000435351.1:p.Gly63Glu
ENST00000527882.5:c.6G>A
ENST00000530998.5:c.299G>A ENSP00000435307.1:p.Gly100Glu
NM_000378.4:c.935G>A NP_000369.3:p.Gly312Glu
NM_001198551.1:c.299G>A , LRG_525t2:c.299G>A NP_001185480.1:p.Gly100Glu
NM_001198552.1:c.299G>A NP_001185481.1:p.Gly100Glu
NM_024424.3:c.935G>A NP_077742.2:p.Gly312Glu
NM_024426.4:c.935G>A NP_077744.3:p.Gly312Glu
NM_000378.5:c.950G>A NP_000369.4:p.Gly317Glu
NM_024424.4:c.950G>A NP_077742.3:p.Gly317Glu
NM_024426.5:c.950G>A NP_077744.4:p.Gly317Glu
NR_160306.1:n.1129G>A
NM_000378.6:c.950G>A NP_000369.4:p.Gly317Glu
NM_001198552.2:c.299G>A NP_001185481.1:p.Gly100Glu
NM_024424.5:c.950G>A NP_077742.3:p.Gly317Glu
NM_024426.6:c.950G>A MANE Select NP_077744.4:p.Gly317Glu