Canonical Allele Identifier: CA379958915

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413582A>C (hg19) ; chr11:g.32392036A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392036A>C , CM000673.2:g.32392036A>C	GRCh38
NC_000011.9:g.32413582A>C , CM000673.1:g.32413582A>C	GRCh37
NC_000011.8:g.32370158A>C	NCBI36
NG_009272.1:g.48506T>G , LRG_525:g.48506T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1332T>G	ENSP00000331327.5:p.Cys444Trp
ENST00000379077.9:c.*567T>G	ENSP00000368368.5:n.*567T>G
ENST00000379079.8:c.732T>G	ENSP00000368370.2:p.Cys244Trp
ENST00000448076.9:c.1383T>G	ENSP00000413452.5:p.Cys461Trp
ENST00000452863.10:c.1383T>G MANE Select	ENSP00000415516.5:p.Cys461Trp
ENST00000526685.2:n.837T>G
ENST00000639563.3:c.1332T>G	ENSP00000492269.3:p.Cys444Trp
ENST00000639907.2:n.526T>G
ENST00000640146.2:c.708T>G	ENSP00000491984.2:p.Cys236Trp
ENST00000650745.1:n.1193T>G
ENST00000650861.1:n.1964T>G
ENST00000650986.1:n.46T>G
ENST00000651459.1:c.154T>G
ENST00000651533.1:n.429T>G
ENST00000651668.1:n.320T>G
ENST00000651794.1:n.1226T>G
ENST00000651819.1:n.308T>G
ENST00000652579.1:n.643T>G
ENST00000652724.1:n.573T>G
ENST00000332351.7:c.1368T>G	ENSP00000331327.3:p.Cys456Trp
ENST00000379077.7:c.*567T>G	ENSP00000368368.3:n.*567T>G
ENST00000379079.6:c.732T>G	ENSP00000368370.2:p.Cys244Trp
ENST00000448076.7:c.1368T>G	ENSP00000413452.3:p.Cys456Trp
ENST00000452863.7:c.1317T>G	ENSP00000415516.3:p.Cys439Trp
ENST00000527882.5:c.349T>G
ENST00000530998.5:c.681T>G	ENSP00000435307.1:p.Cys227Trp
NM_000378.4:c.1317T>G	NP_000369.3:p.Cys439Trp
NM_001198551.1:c.732T>G , LRG_525t2:c.732T>G	NP_001185480.1:p.Cys244Trp
NM_001198552.1:c.681T>G	NP_001185481.1:p.Cys227Trp
NM_024424.3:c.1368T>G	NP_077742.2:p.Cys456Trp
NM_024426.4:c.1368T>G	NP_077744.3:p.Cys456Trp
NM_000378.5:c.1332T>G	NP_000369.4:p.Cys444Trp
NM_024424.4:c.1383T>G	NP_077742.3:p.Cys461Trp
NM_024426.5:c.1383T>G	NP_077744.4:p.Cys461Trp
NM_001367854.1:c.195T>G	NP_001354783.1:p.Cys65Trp
NR_160306.1:n.1715T>G
NM_000378.6:c.1332T>G	NP_000369.4:p.Cys444Trp
NM_001198552.2:c.681T>G	NP_001185481.1:p.Cys227Trp
NM_024424.5:c.1383T>G	NP_077742.3:p.Cys461Trp
NM_024426.6:c.1383T>G MANE Select	NP_077744.4:p.Cys461Trp