Canonical Allele Identifier: CA379959861

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32417845A>T (hg19) ; chr11:g.32396299A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396299A>T , CM000673.2:g.32396299A>T	GRCh38
NC_000011.9:g.32417845A>T , CM000673.1:g.32417845A>T	GRCh37
NC_000011.8:g.32374421A>T	NCBI36
NG_009272.1:g.44243T>A , LRG_525:g.44243T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1171T>A	ENSP00000331327.5:p.Phe391Ile
ENST00000379077.9:c.*406T>A	ENSP00000368368.5:n.*406T>A
ENST00000379079.8:c.571T>A	ENSP00000368370.2:p.Phe191Ile
ENST00000448076.9:c.1222T>A	ENSP00000413452.5:p.Phe408Ile
ENST00000452863.10:c.1222T>A MANE Select	ENSP00000415516.5:p.Phe408Ile
ENST00000526685.2:n.676T>A
ENST00000639563.3:c.1171T>A	ENSP00000492269.3:p.Phe391Ile
ENST00000639907.2:n.365T>A
ENST00000640146.2:c.547T>A	ENSP00000491984.2:p.Phe183Ile
ENST00000650861.1:n.1803T>A
ENST00000651459.1:c.36-3544T>A
ENST00000651668.1:n.159T>A
ENST00000651794.1:n.965T>A
ENST00000651819.1:n.147T>A
ENST00000652579.1:n.382T>A
ENST00000652724.1:n.412T>A
ENST00000332351.7:c.1207T>A	ENSP00000331327.3:p.Phe403Ile
ENST00000379077.7:c.*406T>A	ENSP00000368368.3:n.*406T>A
ENST00000379079.6:c.571T>A	ENSP00000368370.2:p.Phe191Ile
ENST00000448076.7:c.1207T>A	ENSP00000413452.3:p.Phe403Ile
ENST00000452863.7:c.1156T>A	ENSP00000415516.3:p.Phe386Ile
ENST00000526685.1:c.34T>A	ENSP00000436292.1:p.Phe12Ile
ENST00000527882.5:c.278T>A
ENST00000530998.5:c.520T>A	ENSP00000435307.1:p.Phe174Ile
NM_000378.4:c.1156T>A	NP_000369.3:p.Phe386Ile
NM_001198551.1:c.571T>A , LRG_525t2:c.571T>A	NP_001185480.1:p.Phe191Ile
NM_001198552.1:c.520T>A	NP_001185481.1:p.Phe174Ile
NM_024424.3:c.1207T>A	NP_077742.2:p.Phe403Ile
NM_024426.4:c.1207T>A	NP_077744.3:p.Phe403Ile
NM_000378.5:c.1171T>A	NP_000369.4:p.Phe391Ile
NM_024424.4:c.1222T>A	NP_077742.3:p.Phe408Ile
NM_024426.5:c.1222T>A	NP_077744.4:p.Phe408Ile
NM_001367854.1:c.34T>A	NP_001354783.1:p.Phe12Ile
NR_160306.1:n.1554T>A
NM_000378.6:c.1171T>A	NP_000369.4:p.Phe391Ile
NM_001198552.2:c.520T>A	NP_001185481.1:p.Phe174Ile
NM_024424.5:c.1222T>A	NP_077742.3:p.Phe408Ile
NM_024426.6:c.1222T>A MANE Select	NP_077744.4:p.Phe408Ile