Canonical Allele Identifier: CA379959437

Gene: WT1

Linked Data

• dbSNP Id: rs767850636
• MyVariant Identifiers: chr11:g.32414297C>G (hg19) ; chr11:g.32392751C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392751C>G , CM000673.2:g.32392751C>G	GRCh38
NC_000011.9:g.32414297C>G , CM000673.1:g.32414297C>G	GRCh37
NC_000011.8:g.32370873C>G	NCBI36
NG_009272.1:g.47791G>C , LRG_525:g.47791G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1218G>C	ENSP00000331327.5:p.Glu406Asp
ENST00000379077.9:c.*453G>C	ENSP00000368368.5:n.*453G>C
ENST00000379079.8:c.618G>C	ENSP00000368370.2:p.Glu206Asp
ENST00000448076.9:c.1269G>C	ENSP00000413452.5:p.Glu423Asp
ENST00000452863.10:c.1269G>C MANE Select	ENSP00000415516.5:p.Glu423Asp
ENST00000526685.2:n.723G>C
ENST00000639563.3:c.1218G>C	ENSP00000492269.3:p.Glu406Asp
ENST00000639907.2:n.412G>C
ENST00000640146.2:c.594G>C	ENSP00000491984.2:p.Glu198Asp
ENST00000650745.1:n.478G>C
ENST00000650861.1:n.1850G>C
ENST00000651459.1:c.40G>C
ENST00000651533.1:n.315G>C
ENST00000651668.1:n.206G>C
ENST00000651794.1:n.1112G>C
ENST00000651819.1:n.194G>C
ENST00000652579.1:n.529G>C
ENST00000652724.1:n.459G>C
ENST00000332351.7:c.1254G>C	ENSP00000331327.3:p.Glu418Asp
ENST00000379077.7:c.*453G>C	ENSP00000368368.3:n.*453G>C
ENST00000379079.6:c.618G>C	ENSP00000368370.2:p.Glu206Asp
ENST00000448076.7:c.1254G>C	ENSP00000413452.3:p.Glu418Asp
ENST00000452863.7:c.1203G>C	ENSP00000415516.3:p.Glu401Asp
ENST00000527882.5:c.321-687G>C
ENST00000530998.5:c.567G>C	ENSP00000435307.1:p.Glu189Asp
NM_000378.4:c.1203G>C	NP_000369.3:p.Glu401Asp
NM_001198551.1:c.618G>C , LRG_525t2:c.618G>C	NP_001185480.1:p.Glu206Asp
NM_001198552.1:c.567G>C	NP_001185481.1:p.Glu189Asp
NM_024424.3:c.1254G>C	NP_077742.2:p.Glu418Asp
NM_024426.4:c.1254G>C	NP_077744.3:p.Glu418Asp
NM_000378.5:c.1218G>C	NP_000369.4:p.Glu406Asp
NM_024424.4:c.1269G>C	NP_077742.3:p.Glu423Asp
NM_024426.5:c.1269G>C	NP_077744.4:p.Glu423Asp
NM_001367854.1:c.81G>C	NP_001354783.1:p.Glu27Asp
NR_160306.1:n.1601G>C
NM_000378.6:c.1218G>C	NP_000369.4:p.Glu406Asp
NM_001198552.2:c.567G>C	NP_001185481.1:p.Glu189Asp
NM_024424.5:c.1269G>C	NP_077742.3:p.Glu423Asp
NM_024426.6:c.1269G>C MANE Select	NP_077744.4:p.Glu423Asp