Canonical Allele Identifier: CA473565385

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413573C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392027C>T , CM000673.2:g.32392027C>T	GRCh38
NC_000011.9:g.32413573C>T , CM000673.1:g.32413573C>T	GRCh37
NC_000011.8:g.32370149C>T	NCBI36
NG_009272.1:g.48515G>A , LRG_525:g.48515G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1341G>A	ENSP00000331327.5:p.Lys447=
ENST00000379077.9:c.*576G>A	ENSP00000368368.5:n.*576G>A
ENST00000379079.8:c.741G>A	ENSP00000368370.2:p.Lys247=
ENST00000448076.9:c.1392G>A	ENSP00000413452.5:p.Lys464=
ENST00000452863.10:c.1392G>A MANE Select	ENSP00000415516.5:p.Lys464=
ENST00000526685.2:n.846G>A
ENST00000639563.3:c.1341G>A	ENSP00000492269.3:p.Lys447=
ENST00000639907.2:n.535G>A
ENST00000640146.2:c.717G>A	ENSP00000491984.2:p.Lys239=
ENST00000650745.1:n.1202G>A
ENST00000650861.1:n.1973G>A
ENST00000650986.1:n.55G>A
ENST00000651459.1:c.163G>A
ENST00000651533.1:n.438G>A
ENST00000651668.1:n.329G>A
ENST00000651794.1:n.1235G>A
ENST00000651819.1:n.317G>A
ENST00000652579.1:n.652G>A
ENST00000652724.1:n.582G>A
ENST00000332351.7:c.1377G>A	ENSP00000331327.3:p.Lys459=
ENST00000379077.7:c.*576G>A	ENSP00000368368.3:n.*576G>A
ENST00000379079.6:c.741G>A	ENSP00000368370.2:p.Lys247=
ENST00000448076.7:c.1377G>A	ENSP00000413452.3:p.Lys459=
ENST00000452863.7:c.1326G>A	ENSP00000415516.3:p.Lys442=
ENST00000527882.5:c.358G>A
ENST00000530998.5:c.690G>A	ENSP00000435307.1:p.Lys230=
NM_000378.4:c.1326G>A	NP_000369.3:p.Lys442=
NM_001198551.1:c.741G>A , LRG_525t2:c.741G>A	NP_001185480.1:p.Lys247=
NM_001198552.1:c.690G>A	NP_001185481.1:p.Lys230=
NM_024424.3:c.1377G>A	NP_077742.2:p.Lys459=
NM_024426.4:c.1377G>A	NP_077744.3:p.Lys459=
NM_000378.5:c.1341G>A	NP_000369.4:p.Lys447=
NM_024424.4:c.1392G>A	NP_077742.3:p.Lys464=
NM_024426.5:c.1392G>A	NP_077744.4:p.Lys464=
NM_001367854.1:c.204G>A	NP_001354783.1:p.Lys68=
NR_160306.1:n.1724G>A
NM_000378.6:c.1341G>A	NP_000369.4:p.Lys447=
NM_001198552.2:c.690G>A	NP_001185481.1:p.Lys230=
NM_024424.5:c.1392G>A	NP_077742.3:p.Lys464=
NM_024426.6:c.1392G>A MANE Select	NP_077744.4:p.Lys464=