Canonical Allele Identifier: CA473565882

Gene: WT1

Linked Data

• dbSNP Id: rs2132920775
• MyVariant Identifiers: chr11:g.32414267A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392721A>G , CM000673.2:g.32392721A>G	GRCh38
NC_000011.9:g.32414267A>G , CM000673.1:g.32414267A>G	GRCh37
NC_000011.8:g.32370843A>G	NCBI36
NG_009272.1:g.47821T>C , LRG_525:g.47821T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1248T>C	ENSP00000331327.5:p.Cys416=
ENST00000379077.9:c.*483T>C	ENSP00000368368.5:n.*483T>C
ENST00000379079.8:c.648T>C	ENSP00000368370.2:p.Cys216=
ENST00000448076.9:c.1299T>C	ENSP00000413452.5:p.Cys433=
ENST00000452863.10:c.1299T>C MANE Select	ENSP00000415516.5:p.Cys433=
ENST00000526685.2:n.753T>C
ENST00000639563.3:c.1248T>C	ENSP00000492269.3:p.Cys416=
ENST00000639907.2:n.442T>C
ENST00000640146.2:c.624T>C	ENSP00000491984.2:p.Cys208=
ENST00000650745.1:n.508T>C
ENST00000650861.1:n.1880T>C
ENST00000651459.1:c.70T>C
ENST00000651533.1:n.345T>C
ENST00000651668.1:n.236T>C
ENST00000651794.1:n.1142T>C
ENST00000651819.1:n.224T>C
ENST00000652579.1:n.559T>C
ENST00000652724.1:n.489T>C
ENST00000332351.7:c.1284T>C	ENSP00000331327.3:p.Cys428=
ENST00000379077.7:c.*483T>C	ENSP00000368368.3:n.*483T>C
ENST00000379079.6:c.648T>C	ENSP00000368370.2:p.Cys216=
ENST00000448076.7:c.1284T>C	ENSP00000413452.3:p.Cys428=
ENST00000452863.7:c.1233T>C	ENSP00000415516.3:p.Cys411=
ENST00000527882.5:c.321-657T>C
ENST00000530998.5:c.597T>C	ENSP00000435307.1:p.Cys199=
NM_000378.4:c.1233T>C	NP_000369.3:p.Cys411=
NM_001198551.1:c.648T>C , LRG_525t2:c.648T>C	NP_001185480.1:p.Cys216=
NM_001198552.1:c.597T>C	NP_001185481.1:p.Cys199=
NM_024424.3:c.1284T>C	NP_077742.2:p.Cys428=
NM_024426.4:c.1284T>C	NP_077744.3:p.Cys428=
NM_000378.5:c.1248T>C	NP_000369.4:p.Cys416=
NM_024424.4:c.1299T>C	NP_077742.3:p.Cys433=
NM_024426.5:c.1299T>C	NP_077744.4:p.Cys433=
NM_001367854.1:c.111T>C	NP_001354783.1:p.Cys37=
NR_160306.1:n.1631T>C
NM_000378.6:c.1248T>C	NP_000369.4:p.Cys416=
NM_001198552.2:c.597T>C	NP_001185481.1:p.Cys199=
NM_024424.5:c.1299T>C	NP_077742.3:p.Cys433=
NM_024426.6:c.1299T>C MANE Select	NP_077744.4:p.Cys433=