Canonical Allele Identifier: CA379958864

Gene: WT1

Linked Data

• dbSNP Id: rs2132914578
• MyVariant Identifiers: chr11:g.32413569A>T (hg19) ; chr11:g.32392023A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392023A>T , CM000673.2:g.32392023A>T	GRCh38
NC_000011.9:g.32413569A>T , CM000673.1:g.32413569A>T	GRCh37
NC_000011.8:g.32370145A>T	NCBI36
NG_009272.1:g.48519T>A , LRG_525:g.48519T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1345T>A	ENSP00000331327.5:p.Ser449Thr
ENST00000379077.9:c.*580T>A	ENSP00000368368.5:n.*580T>A
ENST00000379079.8:c.745T>A	ENSP00000368370.2:p.Ser249Thr
ENST00000448076.9:c.1396T>A	ENSP00000413452.5:p.Ser466Thr
ENST00000452863.10:c.1396T>A MANE Select	ENSP00000415516.5:p.Ser466Thr
ENST00000526685.2:n.850T>A
ENST00000639563.3:c.1345T>A	ENSP00000492269.3:p.Ser449Thr
ENST00000639907.2:n.539T>A
ENST00000640146.2:c.721T>A	ENSP00000491984.2:p.Ser241Thr
ENST00000650745.1:n.1206T>A
ENST00000650861.1:n.1977T>A
ENST00000650986.1:n.59T>A
ENST00000651459.1:c.167T>A
ENST00000651533.1:n.442T>A
ENST00000651668.1:n.333T>A
ENST00000651794.1:n.1239T>A
ENST00000651819.1:n.321T>A
ENST00000652579.1:n.656T>A
ENST00000652724.1:n.586T>A
ENST00000332351.7:c.1381T>A	ENSP00000331327.3:p.Ser461Thr
ENST00000379077.7:c.*580T>A	ENSP00000368368.3:n.*580T>A
ENST00000379079.6:c.745T>A	ENSP00000368370.2:p.Ser249Thr
ENST00000448076.7:c.1381T>A	ENSP00000413452.3:p.Ser461Thr
ENST00000452863.7:c.1330T>A	ENSP00000415516.3:p.Ser444Thr
ENST00000527882.5:c.362T>A
ENST00000530998.5:c.694T>A	ENSP00000435307.1:p.Ser232Thr
NM_000378.4:c.1330T>A	NP_000369.3:p.Ser444Thr
NM_001198551.1:c.745T>A , LRG_525t2:c.745T>A	NP_001185480.1:p.Ser249Thr
NM_001198552.1:c.694T>A	NP_001185481.1:p.Ser232Thr
NM_024424.3:c.1381T>A	NP_077742.2:p.Ser461Thr
NM_024426.4:c.1381T>A	NP_077744.3:p.Ser461Thr
NM_000378.5:c.1345T>A	NP_000369.4:p.Ser449Thr
NM_024424.4:c.1396T>A	NP_077742.3:p.Ser466Thr
NM_024426.5:c.1396T>A	NP_077744.4:p.Ser466Thr
NM_001367854.1:c.208T>A	NP_001354783.1:p.Ser70Thr
NR_160306.1:n.1728T>A
NM_000378.6:c.1345T>A	NP_000369.4:p.Ser449Thr
NM_001198552.2:c.694T>A	NP_001185481.1:p.Ser232Thr
NM_024424.5:c.1396T>A	NP_077742.3:p.Ser466Thr
NM_024426.6:c.1396T>A MANE Select	NP_077744.4:p.Ser466Thr