Canonical Allele Identifier: CA379959444

Gene: WT1

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392755C>G , CM000673.2:g.32392755C>G	GRCh38
NC_000011.9:g.32414301C>G , CM000673.1:g.32414301C>G	GRCh37
NC_000011.8:g.32370877C>G	NCBI36
NG_009272.1:g.47787G>C , LRG_525:g.47787G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1214G>C	ENSP00000331327.5:p.Gly405Ala
ENST00000379077.9:c.*449G>C	ENSP00000368368.5:n.*449G>C
ENST00000379079.8:c.614G>C	ENSP00000368370.2:p.Gly205Ala
ENST00000448076.9:c.1265G>C	ENSP00000413452.5:p.Gly422Ala
ENST00000452863.10:c.1265G>C MANE Select	ENSP00000415516.5:p.Gly422Ala
ENST00000526685.2:n.719G>C
ENST00000639563.3:c.1214G>C	ENSP00000492269.3:p.Gly405Ala
ENST00000639907.2:n.408G>C
ENST00000640146.2:c.590G>C	ENSP00000491984.2:p.Gly197Ala
ENST00000650745.1:n.474G>C
ENST00000650861.1:n.1846G>C
ENST00000651459.1:c.36G>C
ENST00000651533.1:n.311G>C
ENST00000651668.1:n.202G>C
ENST00000651794.1:n.1108G>C
ENST00000651819.1:n.190G>C
ENST00000652579.1:n.525G>C
ENST00000652724.1:n.455G>C
ENST00000332351.7:c.1250G>C	ENSP00000331327.3:p.Gly417Ala
ENST00000379077.7:c.*449G>C	ENSP00000368368.3:n.*449G>C
ENST00000379079.6:c.614G>C	ENSP00000368370.2:p.Gly205Ala
ENST00000448076.7:c.1250G>C	ENSP00000413452.3:p.Gly417Ala
ENST00000452863.7:c.1199G>C	ENSP00000415516.3:p.Gly400Ala
ENST00000527882.5:c.321-691G>C
ENST00000530998.5:c.563G>C	ENSP00000435307.1:p.Gly188Ala
NM_000378.4:c.1199G>C	NP_000369.3:p.Gly400Ala
NM_001198551.1:c.614G>C , LRG_525t2:c.614G>C	NP_001185480.1:p.Gly205Ala
NM_001198552.1:c.563G>C	NP_001185481.1:p.Gly188Ala
NM_024424.3:c.1250G>C	NP_077742.2:p.Gly417Ala
NM_024426.4:c.1250G>C	NP_077744.3:p.Gly417Ala
NM_000378.5:c.1214G>C	NP_000369.4:p.Gly405Ala
NM_024424.4:c.1265G>C	NP_077742.3:p.Gly422Ala
NM_024426.5:c.1265G>C	NP_077744.4:p.Gly422Ala
NM_001367854.1:c.77G>C	NP_001354783.1:p.Gly26Ala
NR_160306.1:n.1597G>C
NM_000378.6:c.1214G>C	NP_000369.4:p.Gly405Ala
NM_001198552.2:c.563G>C	NP_001185481.1:p.Gly188Ala
NM_024424.5:c.1265G>C	NP_077742.3:p.Gly422Ala
NM_024426.6:c.1265G>C MANE Select	NP_077744.4:p.Gly422Ala