Canonical Allele Identifier: CA379959360
Gene: WT1 HGNC NCBI

Linked Data

dbSNP Id: rs2132921060

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392728T>G , CM000673.2:g.32392728T>G GRCh38
NC_000011.9:g.32414274T>G , CM000673.1:g.32414274T>G GRCh37
NC_000011.8:g.32370850T>G NCBI36
NG_009272.1:g.47814A>C , LRG_525:g.47814A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1241A>C ENSP00000331327.5:p.Lys414Thr
ENST00000379077.9:c.*476A>C ENSP00000368368.5:n.*476A>C
ENST00000379079.8:c.641A>C ENSP00000368370.2:p.Lys214Thr
ENST00000448076.9:c.1292A>C ENSP00000413452.5:p.Lys431Thr
ENST00000452863.10:c.1292A>C MANE Select ENSP00000415516.5:p.Lys431Thr
ENST00000526685.2:n.746A>C
ENST00000639563.3:c.1241A>C ENSP00000492269.3:p.Lys414Thr
ENST00000639907.2:n.435A>C
ENST00000640146.2:c.617A>C ENSP00000491984.2:p.Lys206Thr
ENST00000650745.1:n.501A>C
ENST00000650861.1:n.1873A>C
ENST00000651459.1:c.63A>C
ENST00000651533.1:n.338A>C
ENST00000651668.1:n.229A>C
ENST00000651794.1:n.1135A>C
ENST00000651819.1:n.217A>C
ENST00000652579.1:n.552A>C
ENST00000652724.1:n.482A>C
ENST00000332351.7:c.1277A>C ENSP00000331327.3:p.Lys426Thr
ENST00000379077.7:c.*476A>C ENSP00000368368.3:n.*476A>C
ENST00000379079.6:c.641A>C ENSP00000368370.2:p.Lys214Thr
ENST00000448076.7:c.1277A>C ENSP00000413452.3:p.Lys426Thr
ENST00000452863.7:c.1226A>C ENSP00000415516.3:p.Lys409Thr
ENST00000527882.5:c.321-664A>C
ENST00000530998.5:c.590A>C ENSP00000435307.1:p.Lys197Thr
NM_000378.4:c.1226A>C NP_000369.3:p.Lys409Thr
NM_001198551.1:c.641A>C , LRG_525t2:c.641A>C NP_001185480.1:p.Lys214Thr
NM_001198552.1:c.590A>C NP_001185481.1:p.Lys197Thr
NM_024424.3:c.1277A>C NP_077742.2:p.Lys426Thr
NM_024426.4:c.1277A>C NP_077744.3:p.Lys426Thr
NM_000378.5:c.1241A>C NP_000369.4:p.Lys414Thr
NM_024424.4:c.1292A>C NP_077742.3:p.Lys431Thr
NM_024426.5:c.1292A>C NP_077744.4:p.Lys431Thr
NM_001367854.1:c.104A>C NP_001354783.1:p.Lys35Thr
NR_160306.1:n.1624A>C
NM_000378.6:c.1241A>C NP_000369.4:p.Lys414Thr
NM_001198552.2:c.590A>C NP_001185481.1:p.Lys197Thr
NM_024424.5:c.1292A>C NP_077742.3:p.Lys431Thr
NM_024426.6:c.1292A>C MANE Select NP_077744.4:p.Lys431Thr