Canonical Allele Identifier: CA379958994

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413599A>T (hg19) ; chr11:g.32392053A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392053A>T , CM000673.2:g.32392053A>T	GRCh38
NC_000011.9:g.32413599A>T , CM000673.1:g.32413599A>T	GRCh37
NC_000011.8:g.32370175A>T	NCBI36
NG_009272.1:g.48489T>A , LRG_525:g.48489T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1315T>A	ENSP00000331327.5:p.Phe439Ile
ENST00000379077.9:c.*550T>A	ENSP00000368368.5:n.*550T>A
ENST00000379079.8:c.715T>A	ENSP00000368370.2:p.Phe239Ile
ENST00000448076.9:c.1366T>A	ENSP00000413452.5:p.Phe456Ile
ENST00000452863.10:c.1366T>A MANE Select	ENSP00000415516.5:p.Phe456Ile
ENST00000526685.2:n.820T>A
ENST00000639563.3:c.1315T>A	ENSP00000492269.3:p.Phe439Ile
ENST00000639907.2:n.509T>A
ENST00000640146.2:c.691T>A	ENSP00000491984.2:p.Phe231Ile
ENST00000650745.1:n.1176T>A
ENST00000650861.1:n.1947T>A
ENST00000650986.1:n.29T>A
ENST00000651459.1:c.137T>A
ENST00000651533.1:n.412T>A
ENST00000651668.1:n.303T>A
ENST00000651794.1:n.1209T>A
ENST00000651819.1:n.291T>A
ENST00000652579.1:n.626T>A
ENST00000652724.1:n.556T>A
ENST00000332351.7:c.1351T>A	ENSP00000331327.3:p.Phe451Ile
ENST00000379077.7:c.*550T>A	ENSP00000368368.3:n.*550T>A
ENST00000379079.6:c.715T>A	ENSP00000368370.2:p.Phe239Ile
ENST00000448076.7:c.1351T>A	ENSP00000413452.3:p.Phe451Ile
ENST00000452863.7:c.1300T>A	ENSP00000415516.3:p.Phe434Ile
ENST00000527882.5:c.332T>A
ENST00000530998.5:c.664T>A	ENSP00000435307.1:p.Phe222Ile
NM_000378.4:c.1300T>A	NP_000369.3:p.Phe434Ile
NM_001198551.1:c.715T>A , LRG_525t2:c.715T>A	NP_001185480.1:p.Phe239Ile
NM_001198552.1:c.664T>A	NP_001185481.1:p.Phe222Ile
NM_024424.3:c.1351T>A	NP_077742.2:p.Phe451Ile
NM_024426.4:c.1351T>A	NP_077744.3:p.Phe451Ile
NM_000378.5:c.1315T>A	NP_000369.4:p.Phe439Ile
NM_024424.4:c.1366T>A	NP_077742.3:p.Phe456Ile
NM_024426.5:c.1366T>A	NP_077744.4:p.Phe456Ile
NM_001367854.1:c.178T>A	NP_001354783.1:p.Phe60Ile
NR_160306.1:n.1698T>A
NM_000378.6:c.1315T>A	NP_000369.4:p.Phe439Ile
NM_001198552.2:c.664T>A	NP_001185481.1:p.Phe222Ile
NM_024424.5:c.1366T>A	NP_077742.3:p.Phe456Ile
NM_024426.6:c.1366T>A MANE Select	NP_077744.4:p.Phe456Ile