Canonical Allele Identifier: CA473565329

Gene: WT1

Linked Data

• dbSNP Id: rs2132914147
• MyVariant Identifiers: chr11:g.32413552C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392006C>G , CM000673.2:g.32392006C>G	GRCh38
NC_000011.9:g.32413552C>G , CM000673.1:g.32413552C>G	GRCh37
NC_000011.8:g.32370128C>G	NCBI36
NG_009272.1:g.48536G>C , LRG_525:g.48536G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1362G>C	ENSP00000331327.5:p.Leu454=
ENST00000379077.9:c.*597G>C	ENSP00000368368.5:n.*597G>C
ENST00000379079.8:c.762G>C	ENSP00000368370.2:p.Leu254=
ENST00000448076.9:c.1413G>C	ENSP00000413452.5:p.Leu471=
ENST00000452863.10:c.1413G>C MANE Select	ENSP00000415516.5:p.Leu471=
ENST00000526685.2:n.867G>C
ENST00000639563.3:c.1362G>C	ENSP00000492269.3:p.Leu454=
ENST00000639907.2:n.556G>C
ENST00000640146.2:c.738G>C	ENSP00000491984.2:p.Leu246=
ENST00000650745.1:n.1223G>C
ENST00000650861.1:n.1994G>C
ENST00000650986.1:n.76G>C
ENST00000651459.1:c.184G>C
ENST00000651533.1:n.459G>C
ENST00000651668.1:n.350G>C
ENST00000651794.1:n.1256G>C
ENST00000651819.1:n.338G>C
ENST00000652579.1:n.673G>C
ENST00000652724.1:n.603G>C
ENST00000332351.7:c.1398G>C	ENSP00000331327.3:p.Leu466=
ENST00000379077.7:c.*597G>C	ENSP00000368368.3:n.*597G>C
ENST00000379079.6:c.762G>C	ENSP00000368370.2:p.Leu254=
ENST00000448076.7:c.1398G>C	ENSP00000413452.3:p.Leu466=
ENST00000452863.7:c.1347G>C	ENSP00000415516.3:p.Leu449=
ENST00000527882.5:c.379G>C
ENST00000530998.5:c.711G>C	ENSP00000435307.1:p.Leu237=
NM_000378.4:c.1347G>C	NP_000369.3:p.Leu449=
NM_001198551.1:c.762G>C , LRG_525t2:c.762G>C	NP_001185480.1:p.Leu254=
NM_001198552.1:c.711G>C	NP_001185481.1:p.Leu237=
NM_024424.3:c.1398G>C	NP_077742.2:p.Leu466=
NM_024426.4:c.1398G>C	NP_077744.3:p.Leu466=
NM_000378.5:c.1362G>C	NP_000369.4:p.Leu454=
NM_024424.4:c.1413G>C	NP_077742.3:p.Leu471=
NM_024426.5:c.1413G>C	NP_077744.4:p.Leu471=
NM_001367854.1:c.225G>C	NP_001354783.1:p.Leu75=
NR_160306.1:n.1745G>C
NM_000378.6:c.1362G>C	NP_000369.4:p.Leu454=
NM_001198552.2:c.711G>C	NP_001185481.1:p.Leu237=
NM_024424.5:c.1413G>C	NP_077742.3:p.Leu471=
NM_024426.6:c.1413G>C MANE Select	NP_077744.4:p.Leu471=