Canonical Allele Identifier: CA379958858

Gene: WT1

Linked Data

• dbSNP Id: rs1421664466
• gnomAD v2: 11-32413568-G-A
• gnomAD v3: 11-32392022-G-A
• gnomAD v4: 11-32392022-G-A
• MyVariant Identifiers: chr11:g.32413568G>A (hg19) ; chr11:g.32392022G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392022G>A , CM000673.2:g.32392022G>A	GRCh38
NC_000011.9:g.32413568G>A , CM000673.1:g.32413568G>A	GRCh37
NC_000011.8:g.32370144G>A	NCBI36
NG_009272.1:g.48520C>T , LRG_525:g.48520C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1346C>T	ENSP00000331327.5:p.Ser449Phe
ENST00000379077.9:c.*581C>T	ENSP00000368368.5:n.*581C>T
ENST00000379079.8:c.746C>T	ENSP00000368370.2:p.Ser249Phe
ENST00000448076.9:c.1397C>T	ENSP00000413452.5:p.Ser466Phe
ENST00000452863.10:c.1397C>T MANE Select	ENSP00000415516.5:p.Ser466Phe
ENST00000526685.2:n.851C>T
ENST00000639563.3:c.1346C>T	ENSP00000492269.3:p.Ser449Phe
ENST00000639907.2:n.540C>T
ENST00000640146.2:c.722C>T	ENSP00000491984.2:p.Ser241Phe
ENST00000650745.1:n.1207C>T
ENST00000650861.1:n.1978C>T
ENST00000650986.1:n.60C>T
ENST00000651459.1:c.168C>T
ENST00000651533.1:n.443C>T
ENST00000651668.1:n.334C>T
ENST00000651794.1:n.1240C>T
ENST00000651819.1:n.322C>T
ENST00000652579.1:n.657C>T
ENST00000652724.1:n.587C>T
ENST00000332351.7:c.1382C>T	ENSP00000331327.3:p.Ser461Phe
ENST00000379077.7:c.*581C>T	ENSP00000368368.3:n.*581C>T
ENST00000379079.6:c.746C>T	ENSP00000368370.2:p.Ser249Phe
ENST00000448076.7:c.1382C>T	ENSP00000413452.3:p.Ser461Phe
ENST00000452863.7:c.1331C>T	ENSP00000415516.3:p.Ser444Phe
ENST00000527882.5:c.363C>T
ENST00000530998.5:c.695C>T	ENSP00000435307.1:p.Ser232Phe
NM_000378.4:c.1331C>T	NP_000369.3:p.Ser444Phe
NM_001198551.1:c.746C>T , LRG_525t2:c.746C>T	NP_001185480.1:p.Ser249Phe
NM_001198552.1:c.695C>T	NP_001185481.1:p.Ser232Phe
NM_024424.3:c.1382C>T	NP_077742.2:p.Ser461Phe
NM_024426.4:c.1382C>T	NP_077744.3:p.Ser461Phe
NM_000378.5:c.1346C>T	NP_000369.4:p.Ser449Phe
NM_024424.4:c.1397C>T	NP_077742.3:p.Ser466Phe
NM_024426.5:c.1397C>T	NP_077744.4:p.Ser466Phe
NM_001367854.1:c.209C>T	NP_001354783.1:p.Ser70Phe
NR_160306.1:n.1729C>T
NM_000378.6:c.1346C>T	NP_000369.4:p.Ser449Phe
NM_001198552.2:c.695C>T	NP_001185481.1:p.Ser232Phe
NM_024424.5:c.1397C>T	NP_077742.3:p.Ser466Phe
NM_024426.6:c.1397C>T MANE Select	NP_077744.4:p.Ser466Phe