Canonical Allele Identifier: CA379958754

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413542T>C (hg19) ; chr11:g.32391996T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391996T>C , CM000673.2:g.32391996T>C	GRCh38
NC_000011.9:g.32413542T>C , CM000673.1:g.32413542T>C	GRCh37
NC_000011.8:g.32370118T>C	NCBI36
NG_009272.1:g.48546A>G , LRG_525:g.48546A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1372A>G	ENSP00000331327.5:p.Thr458Ala
ENST00000379077.9:c.*607A>G	ENSP00000368368.5:n.*607A>G
ENST00000379079.8:c.772A>G	ENSP00000368370.2:p.Thr258Ala
ENST00000448076.9:c.1423A>G	ENSP00000413452.5:p.Thr475Ala
ENST00000452863.10:c.1423A>G MANE Select	ENSP00000415516.5:p.Thr475Ala
ENST00000526685.2:n.877A>G
ENST00000639563.3:c.1372A>G	ENSP00000492269.3:p.Thr458Ala
ENST00000639907.2:n.566A>G
ENST00000640146.2:c.748A>G	ENSP00000491984.2:p.Thr250Ala
ENST00000650745.1:n.1233A>G
ENST00000650861.1:n.2004A>G
ENST00000650986.1:n.86A>G
ENST00000651459.1:c.194A>G
ENST00000651533.1:n.469A>G
ENST00000651668.1:n.360A>G
ENST00000651794.1:n.1266A>G
ENST00000651819.1:n.348A>G
ENST00000652579.1:n.683A>G
ENST00000652724.1:n.613A>G
ENST00000332351.7:c.1408A>G	ENSP00000331327.3:p.Thr470Ala
ENST00000379077.7:c.*607A>G	ENSP00000368368.3:n.*607A>G
ENST00000379079.6:c.772A>G	ENSP00000368370.2:p.Thr258Ala
ENST00000448076.7:c.1408A>G	ENSP00000413452.3:p.Thr470Ala
ENST00000452863.7:c.1357A>G	ENSP00000415516.3:p.Thr453Ala
ENST00000527882.5:c.389A>G
ENST00000530998.5:c.721A>G	ENSP00000435307.1:p.Thr241Ala
NM_000378.4:c.1357A>G	NP_000369.3:p.Thr453Ala
NM_001198551.1:c.772A>G , LRG_525t2:c.772A>G	NP_001185480.1:p.Thr258Ala
NM_001198552.1:c.721A>G	NP_001185481.1:p.Thr241Ala
NM_024424.3:c.1408A>G	NP_077742.2:p.Thr470Ala
NM_024426.4:c.1408A>G	NP_077744.3:p.Thr470Ala
NM_000378.5:c.1372A>G	NP_000369.4:p.Thr458Ala
NM_024424.4:c.1423A>G	NP_077742.3:p.Thr475Ala
NM_024426.5:c.1423A>G	NP_077744.4:p.Thr475Ala
NM_001367854.1:c.235A>G	NP_001354783.1:p.Thr79Ala
NR_160306.1:n.1755A>G
NM_000378.6:c.1372A>G	NP_000369.4:p.Thr458Ala
NM_001198552.2:c.721A>G	NP_001185481.1:p.Thr241Ala
NM_024424.5:c.1423A>G	NP_077742.3:p.Thr475Ala
NM_024426.6:c.1423A>G MANE Select	NP_077744.4:p.Thr475Ala