Canonical Allele Identifier: CA473773757
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2953624
ClinVar RCV Id: RCV003812847
MyVariant Identifiers: chr11:g.32456537A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32434991A>G , CM000673.2:g.32434991A>G GRCh38
NC_000011.9:g.32456537A>G , CM000673.1:g.32456537A>G GRCh37
NC_000011.8:g.32413113A>G NCBI36
NG_009272.1:g.5551T>C , LRG_525:g.5551T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.370T>C ENSP00000331327.5:p.Leu124=
ENST00000379077.9:c.370T>C ENSP00000368368.5:p.Leu124=
ENST00000448076.9:c.370T>C ENSP00000413452.5:p.Leu124=
ENST00000452863.10:c.370T>C MANE Select ENSP00000415516.5:p.Leu124=
ENST00000639563.3:c.370T>C ENSP00000492269.3:p.Leu124=
ENST00000332351.7:c.355T>C ENSP00000331327.3:p.Leu119=
ENST00000379077.7:c.355T>C ENSP00000368368.3:p.Leu119=
ENST00000448076.7:c.355T>C ENSP00000413452.3:p.Leu119=
ENST00000452863.7:c.355T>C ENSP00000415516.3:p.Leu119=
NM_000378.4:c.355T>C NP_000369.3:p.Leu119=
NM_024424.3:c.355T>C NP_077742.2:p.Leu119=
NM_024426.4:c.355T>C NP_077744.3:p.Leu119=
NM_000378.5:c.370T>C NP_000369.4:p.Leu124=
NM_024424.4:c.370T>C NP_077742.3:p.Leu124=
NM_024426.5:c.370T>C NP_077744.4:p.Leu124=
NR_160306.1:n.549T>C
NM_000378.6:c.370T>C NP_000369.4:p.Leu124=
NM_024424.5:c.370T>C NP_077742.3:p.Leu124=
NM_024426.6:c.370T>C MANE Select NP_077744.4:p.Leu124=