Canonical Allele Identifier: CA379958650

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413518T>C (hg19) ; chr11:g.32391972T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391972T>C , CM000673.2:g.32391972T>C	GRCh38
NC_000011.9:g.32413518T>C , CM000673.1:g.32413518T>C	GRCh37
NC_000011.8:g.32370094T>C	NCBI36
NG_009272.1:g.48570A>G , LRG_525:g.48570A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1387+9A>G	ENSP00000331327.5:n.1387+9A>G
ENST00000379077.9:c.*631A>G	ENSP00000368368.5:n.*631A>G
ENST00000379079.8:c.787+9A>G	ENSP00000368370.2:n.787+9A>G
ENST00000448076.9:c.1438+9A>G	ENSP00000413452.5:n.1438+9A>G
ENST00000452863.10:c.1447A>G MANE Select	ENSP00000415516.5:p.Ser483Gly
ENST00000526685.2:n.892+9A>G
ENST00000639563.3:c.1396A>G	ENSP00000492269.3:p.Ser466Gly
ENST00000639907.2:n.581+9A>G
ENST00000640146.2:c.772A>G	ENSP00000491984.2:p.Ser258Gly
ENST00000650745.1:n.1257A>G
ENST00000650861.1:n.2019+9A>G
ENST00000650986.1:n.110A>G
ENST00000651459.1:c.218A>G
ENST00000651533.1:n.484+9A>G
ENST00000651668.1:n.384A>G
ENST00000651794.1:n.1290A>G
ENST00000651819.1:n.372A>G
ENST00000652579.1:n.707A>G
ENST00000652724.1:n.637A>G
ENST00000332351.7:c.1432A>G	ENSP00000331327.3:p.Ser478Gly
ENST00000379077.7:c.*631A>G	ENSP00000368368.3:n.*631A>G
ENST00000379079.6:c.787+9A>G	ENSP00000368370.2:n.787+9A>G
ENST00000448076.7:c.1423+9A>G	ENSP00000413452.3:n.1423+9A>G
ENST00000452863.7:c.1372+9A>G	ENSP00000415516.3:n.1372+9A>G
ENST00000527882.5:c.413A>G
ENST00000530998.5:c.745A>G	ENSP00000435307.1:p.Ser249Gly
NM_000378.4:c.1372+9A>G	NP_000369.3:n.1372+9A>G
NM_001198551.1:c.787+9A>G , LRG_525t2:c.787+9A>G	NP_001185480.1:n.787+9A>G
NM_001198552.1:c.745A>G	NP_001185481.1:p.Ser249Gly
NM_024424.3:c.1423+9A>G	NP_077742.2:n.1423+9A>G
NM_024426.4:c.1432A>G	NP_077744.3:p.Ser478Gly
NM_000378.5:c.1387+9A>G	NP_000369.4:n.1387+9A>G
NM_024424.4:c.1438+9A>G	NP_077742.3:n.1438+9A>G
NM_024426.5:c.1447A>G	NP_077744.4:p.Ser483Gly
NM_001367854.1:c.259A>G	NP_001354783.1:p.Ser87Gly
NR_160306.1:n.1779A>G
NM_000378.6:c.1387+9A>G	NP_000369.4:n.1387+9A>G
NM_001198552.2:c.745A>G	NP_001185481.1:p.Ser249Gly
NM_024424.5:c.1438+9A>G	NP_077742.3:n.1438+9A>G
NM_024426.6:c.1447A>G MANE Select	NP_077744.4:p.Ser483Gly