Canonical Allele Identifier: CA379966049
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1502337
dbSNP Id: rs1410971862

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32435099C>T , CM000673.2:g.32435099C>T GRCh38
NC_000011.9:g.32456645C>T , CM000673.1:g.32456645C>T GRCh37
NC_000011.8:g.32413221C>T NCBI36
NG_009272.1:g.5443G>A , LRG_525:g.5443G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.262G>A ENSP00000331327.5:p.Val88Ile
ENST00000379077.9:c.262G>A ENSP00000368368.5:p.Val88Ile
ENST00000448076.9:c.262G>A ENSP00000413452.5:p.Val88Ile
ENST00000452863.10:c.262G>A MANE Select ENSP00000415516.5:p.Val88Ile
ENST00000639563.3:c.262G>A ENSP00000492269.3:p.Val88Ile
ENST00000332351.7:c.247G>A ENSP00000331327.3:p.Val83Ile
ENST00000379077.7:c.247G>A ENSP00000368368.3:p.Val83Ile
ENST00000448076.7:c.247G>A ENSP00000413452.3:p.Val83Ile
ENST00000452863.7:c.247G>A ENSP00000415516.3:p.Val83Ile
NM_000378.4:c.247G>A NP_000369.3:p.Val83Ile
NM_024424.3:c.247G>A NP_077742.2:p.Val83Ile
NM_024426.4:c.247G>A NP_077744.3:p.Val83Ile
NM_000378.5:c.262G>A NP_000369.4:p.Val88Ile
NM_024424.4:c.262G>A NP_077742.3:p.Val88Ile
NM_024426.5:c.262G>A NP_077744.4:p.Val88Ile
NR_160306.1:n.441G>A
NM_000378.6:c.262G>A NP_000369.4:p.Val88Ile
NM_024424.5:c.262G>A NP_077742.3:p.Val88Ile
NM_024426.6:c.262G>A MANE Select NP_077744.4:p.Val88Ile