Canonical Allele Identifier: CA064867
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 261711
dbSNP Id: rs771681406

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32434980G>C , CM000673.2:g.32434980G>C GRCh38
NC_000011.9:g.32456526G>C , CM000673.1:g.32456526G>C GRCh37
NC_000011.8:g.32413102G>C NCBI36
NG_009272.1:g.5562C>G , LRG_525:g.5562C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.381C>G ENSP00000331327.5:p.Pro127=
ENST00000379077.9:c.381C>G ENSP00000368368.5:p.Pro127=
ENST00000448076.9:c.381C>G ENSP00000413452.5:p.Pro127=
ENST00000452863.10:c.381C>G MANE Select ENSP00000415516.5:p.Pro127=
ENST00000639563.3:c.381C>G ENSP00000492269.3:p.Pro127=
ENST00000332351.7:c.366C>G ENSP00000331327.3:p.Pro122=
ENST00000379077.7:c.366C>G ENSP00000368368.3:p.Pro122=
ENST00000448076.7:c.366C>G ENSP00000413452.3:p.Pro122=
ENST00000452863.7:c.366C>G ENSP00000415516.3:p.Pro122=
NM_000378.4:c.366C>G NP_000369.3:p.Pro122=
NM_024424.3:c.366C>G NP_077742.2:p.Pro122=
NM_024426.4:c.366C>G NP_077744.3:p.Pro122=
NM_000378.5:c.381C>G NP_000369.4:p.Pro127=
NM_024424.4:c.381C>G NP_077742.3:p.Pro127=
NM_024426.5:c.381C>G NP_077744.4:p.Pro127=
NR_160306.1:n.560C>G
NM_000378.6:c.381C>G NP_000369.4:p.Pro127=
NM_024424.5:c.381C>G NP_077742.3:p.Pro127=
NM_024426.6:c.381C>G MANE Select NP_077744.4:p.Pro127=