Canonical Allele Identifier: CA379959135

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32414219T>G (hg19) ; chr11:g.32392673T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392673T>G , CM000673.2:g.32392673T>G	GRCh38
NC_000011.9:g.32414219T>G , CM000673.1:g.32414219T>G	GRCh37
NC_000011.8:g.32370795T>G	NCBI36
NG_009272.1:g.47869A>C , LRG_525:g.47869A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1296A>C	ENSP00000331327.5:p.Arg432Ser
ENST00000379077.9:c.*531A>C	ENSP00000368368.5:n.*531A>C
ENST00000379079.8:c.696A>C	ENSP00000368370.2:p.Arg232Ser
ENST00000448076.9:c.1347A>C	ENSP00000413452.5:p.Arg449Ser
ENST00000452863.10:c.1347A>C MANE Select	ENSP00000415516.5:p.Arg449Ser
ENST00000526685.2:n.801A>C
ENST00000639563.3:c.1296A>C	ENSP00000492269.3:p.Arg432Ser
ENST00000639907.2:n.490A>C
ENST00000640146.2:c.672A>C	ENSP00000491984.2:p.Arg224Ser
ENST00000650745.1:n.556A>C
ENST00000650861.1:n.1928A>C
ENST00000651459.1:c.118A>C
ENST00000651533.1:n.393A>C
ENST00000651668.1:n.284A>C
ENST00000651794.1:n.1190A>C
ENST00000651819.1:n.272A>C
ENST00000652579.1:n.607A>C
ENST00000652724.1:n.537A>C
ENST00000332351.7:c.1332A>C	ENSP00000331327.3:p.Arg444Ser
ENST00000379077.7:c.*531A>C	ENSP00000368368.3:n.*531A>C
ENST00000379079.6:c.696A>C	ENSP00000368370.2:p.Arg232Ser
ENST00000448076.7:c.1332A>C	ENSP00000413452.3:p.Arg444Ser
ENST00000452863.7:c.1281A>C	ENSP00000415516.3:p.Arg427Ser
ENST00000527882.5:c.321-609A>C
ENST00000530998.5:c.645A>C	ENSP00000435307.1:p.Arg215Ser
NM_000378.4:c.1281A>C	NP_000369.3:p.Arg427Ser
NM_001198551.1:c.696A>C , LRG_525t2:c.696A>C	NP_001185480.1:p.Arg232Ser
NM_001198552.1:c.645A>C	NP_001185481.1:p.Arg215Ser
NM_024424.3:c.1332A>C	NP_077742.2:p.Arg444Ser
NM_024426.4:c.1332A>C	NP_077744.3:p.Arg444Ser
NM_000378.5:c.1296A>C	NP_000369.4:p.Arg432Ser
NM_024424.4:c.1347A>C	NP_077742.3:p.Arg449Ser
NM_024426.5:c.1347A>C	NP_077744.4:p.Arg449Ser
NM_001367854.1:c.159A>C	NP_001354783.1:p.Arg53Ser
NR_160306.1:n.1679A>C
NM_000378.6:c.1296A>C	NP_000369.4:p.Arg432Ser
NM_001198552.2:c.645A>C	NP_001185481.1:p.Arg215Ser
NM_024424.5:c.1347A>C	NP_077742.3:p.Arg449Ser
NM_024426.6:c.1347A>C MANE Select	NP_077744.4:p.Arg449Ser