Canonical Allele Identifier: CA379959343

Gene: WT1

Linked Data

• dbSNP Id: rs2132920946
• MyVariant Identifiers: chr11:g.32414271T>A (hg19) ; chr11:g.32392725T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392725T>A , CM000673.2:g.32392725T>A	GRCh38
NC_000011.9:g.32414271T>A , CM000673.1:g.32414271T>A	GRCh37
NC_000011.8:g.32370847T>A	NCBI36
NG_009272.1:g.47817A>T , LRG_525:g.47817A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1244A>T	ENSP00000331327.5:p.Asp415Val
ENST00000379077.9:c.*479A>T	ENSP00000368368.5:n.*479A>T
ENST00000379079.8:c.644A>T	ENSP00000368370.2:p.Asp215Val
ENST00000448076.9:c.1295A>T	ENSP00000413452.5:p.Asp432Val
ENST00000452863.10:c.1295A>T MANE Select	ENSP00000415516.5:p.Asp432Val
ENST00000526685.2:n.749A>T
ENST00000639563.3:c.1244A>T	ENSP00000492269.3:p.Asp415Val
ENST00000639907.2:n.438A>T
ENST00000640146.2:c.620A>T	ENSP00000491984.2:p.Asp207Val
ENST00000650745.1:n.504A>T
ENST00000650861.1:n.1876A>T
ENST00000651459.1:c.66A>T
ENST00000651533.1:n.341A>T
ENST00000651668.1:n.232A>T
ENST00000651794.1:n.1138A>T
ENST00000651819.1:n.220A>T
ENST00000652579.1:n.555A>T
ENST00000652724.1:n.485A>T
ENST00000332351.7:c.1280A>T	ENSP00000331327.3:p.Asp427Val
ENST00000379077.7:c.*479A>T	ENSP00000368368.3:n.*479A>T
ENST00000379079.6:c.644A>T	ENSP00000368370.2:p.Asp215Val
ENST00000448076.7:c.1280A>T	ENSP00000413452.3:p.Asp427Val
ENST00000452863.7:c.1229A>T	ENSP00000415516.3:p.Asp410Val
ENST00000527882.5:c.321-661A>T
ENST00000530998.5:c.593A>T	ENSP00000435307.1:p.Asp198Val
NM_000378.4:c.1229A>T	NP_000369.3:p.Asp410Val
NM_001198551.1:c.644A>T , LRG_525t2:c.644A>T	NP_001185480.1:p.Asp215Val
NM_001198552.1:c.593A>T	NP_001185481.1:p.Asp198Val
NM_024424.3:c.1280A>T	NP_077742.2:p.Asp427Val
NM_024426.4:c.1280A>T	NP_077744.3:p.Asp427Val
NM_000378.5:c.1244A>T	NP_000369.4:p.Asp415Val
NM_024424.4:c.1295A>T	NP_077742.3:p.Asp432Val
NM_024426.5:c.1295A>T	NP_077744.4:p.Asp432Val
NM_001367854.1:c.107A>T	NP_001354783.1:p.Asp36Val
NR_160306.1:n.1627A>T
NM_000378.6:c.1244A>T	NP_000369.4:p.Asp415Val
NM_001198552.2:c.593A>T	NP_001185481.1:p.Asp198Val
NM_024424.5:c.1295A>T	NP_077742.3:p.Asp432Val
NM_024426.6:c.1295A>T MANE Select	NP_077744.4:p.Asp432Val