Canonical Allele Identifier: CA379959342

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32414270G>T (hg19) ; chr11:g.32392724G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392724G>T , CM000673.2:g.32392724G>T	GRCh38
NC_000011.9:g.32414270G>T , CM000673.1:g.32414270G>T	GRCh37
NC_000011.8:g.32370846G>T	NCBI36
NG_009272.1:g.47818C>A , LRG_525:g.47818C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1245C>A	ENSP00000331327.5:p.Asp415Glu
ENST00000379077.9:c.*480C>A	ENSP00000368368.5:n.*480C>A
ENST00000379079.8:c.645C>A	ENSP00000368370.2:p.Asp215Glu
ENST00000448076.9:c.1296C>A	ENSP00000413452.5:p.Asp432Glu
ENST00000452863.10:c.1296C>A MANE Select	ENSP00000415516.5:p.Asp432Glu
ENST00000526685.2:n.750C>A
ENST00000639563.3:c.1245C>A	ENSP00000492269.3:p.Asp415Glu
ENST00000639907.2:n.439C>A
ENST00000640146.2:c.621C>A	ENSP00000491984.2:p.Asp207Glu
ENST00000650745.1:n.505C>A
ENST00000650861.1:n.1877C>A
ENST00000651459.1:c.67C>A
ENST00000651533.1:n.342C>A
ENST00000651668.1:n.233C>A
ENST00000651794.1:n.1139C>A
ENST00000651819.1:n.221C>A
ENST00000652579.1:n.556C>A
ENST00000652724.1:n.486C>A
ENST00000332351.7:c.1281C>A	ENSP00000331327.3:p.Asp427Glu
ENST00000379077.7:c.*480C>A	ENSP00000368368.3:n.*480C>A
ENST00000379079.6:c.645C>A	ENSP00000368370.2:p.Asp215Glu
ENST00000448076.7:c.1281C>A	ENSP00000413452.3:p.Asp427Glu
ENST00000452863.7:c.1230C>A	ENSP00000415516.3:p.Asp410Glu
ENST00000527882.5:c.321-660C>A
ENST00000530998.5:c.594C>A	ENSP00000435307.1:p.Asp198Glu
NM_000378.4:c.1230C>A	NP_000369.3:p.Asp410Glu
NM_001198551.1:c.645C>A , LRG_525t2:c.645C>A	NP_001185480.1:p.Asp215Glu
NM_001198552.1:c.594C>A	NP_001185481.1:p.Asp198Glu
NM_024424.3:c.1281C>A	NP_077742.2:p.Asp427Glu
NM_024426.4:c.1281C>A	NP_077744.3:p.Asp427Glu
NM_000378.5:c.1245C>A	NP_000369.4:p.Asp415Glu
NM_024424.4:c.1296C>A	NP_077742.3:p.Asp432Glu
NM_024426.5:c.1296C>A	NP_077744.4:p.Asp432Glu
NM_001367854.1:c.108C>A	NP_001354783.1:p.Asp36Glu
NR_160306.1:n.1628C>A
NM_000378.6:c.1245C>A	NP_000369.4:p.Asp415Glu
NM_001198552.2:c.594C>A	NP_001185481.1:p.Asp198Glu
NM_024424.5:c.1296C>A	NP_077742.3:p.Asp432Glu
NM_024426.6:c.1296C>A MANE Select	NP_077744.4:p.Asp432Glu