Canonical Allele Identifier: CA473565364

Gene: WT1

Linked Data

• ClinVar Variation Id: 1613275
• ClinVar RCV Id: RCV002158207
• dbSNP Id: rs2132914457
• MyVariant Identifiers: chr11:g.32413564C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392018C>T , CM000673.2:g.32392018C>T	GRCh38
NC_000011.9:g.32413564C>T , CM000673.1:g.32413564C>T	GRCh37
NC_000011.8:g.32370140C>T	NCBI36
NG_009272.1:g.48524G>A , LRG_525:g.48524G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1350G>A	ENSP00000331327.5:p.Arg450=
ENST00000379077.9:c.*585G>A	ENSP00000368368.5:n.*585G>A
ENST00000379079.8:c.750G>A	ENSP00000368370.2:p.Arg250=
ENST00000448076.9:c.1401G>A	ENSP00000413452.5:p.Arg467=
ENST00000452863.10:c.1401G>A MANE Select	ENSP00000415516.5:p.Arg467=
ENST00000526685.2:n.855G>A
ENST00000639563.3:c.1350G>A	ENSP00000492269.3:p.Arg450=
ENST00000639907.2:n.544G>A
ENST00000640146.2:c.726G>A	ENSP00000491984.2:p.Arg242=
ENST00000650745.1:n.1211G>A
ENST00000650861.1:n.1982G>A
ENST00000650986.1:n.64G>A
ENST00000651459.1:c.172G>A
ENST00000651533.1:n.447G>A
ENST00000651668.1:n.338G>A
ENST00000651794.1:n.1244G>A
ENST00000651819.1:n.326G>A
ENST00000652579.1:n.661G>A
ENST00000652724.1:n.591G>A
ENST00000332351.7:c.1386G>A	ENSP00000331327.3:p.Arg462=
ENST00000379077.7:c.*585G>A	ENSP00000368368.3:n.*585G>A
ENST00000379079.6:c.750G>A	ENSP00000368370.2:p.Arg250=
ENST00000448076.7:c.1386G>A	ENSP00000413452.3:p.Arg462=
ENST00000452863.7:c.1335G>A	ENSP00000415516.3:p.Arg445=
ENST00000527882.5:c.367G>A
ENST00000530998.5:c.699G>A	ENSP00000435307.1:p.Arg233=
NM_000378.4:c.1335G>A	NP_000369.3:p.Arg445=
NM_001198551.1:c.750G>A , LRG_525t2:c.750G>A	NP_001185480.1:p.Arg250=
NM_001198552.1:c.699G>A	NP_001185481.1:p.Arg233=
NM_024424.3:c.1386G>A	NP_077742.2:p.Arg462=
NM_024426.4:c.1386G>A	NP_077744.3:p.Arg462=
NM_000378.5:c.1350G>A	NP_000369.4:p.Arg450=
NM_024424.4:c.1401G>A	NP_077742.3:p.Arg467=
NM_024426.5:c.1401G>A	NP_077744.4:p.Arg467=
NM_001367854.1:c.213G>A	NP_001354783.1:p.Arg71=
NR_160306.1:n.1733G>A
NM_000378.6:c.1350G>A	NP_000369.4:p.Arg450=
NM_001198552.2:c.699G>A	NP_001185481.1:p.Arg233=
NM_024424.5:c.1401G>A	NP_077742.3:p.Arg467=
NM_024426.6:c.1401G>A MANE Select	NP_077744.4:p.Arg467=