Canonical Allele Identifier: CA379959892

Gene: WT1

Linked Data

• dbSNP Id: rs121907904
• MyVariant Identifiers: chr11:g.32417859C>G (hg19) ; chr11:g.32396313C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396313C>G , CM000673.2:g.32396313C>G	GRCh38
NC_000011.9:g.32417859C>G , CM000673.1:g.32417859C>G	GRCh37
NC_000011.8:g.32374435C>G	NCBI36
NG_009272.1:g.44229G>C , LRG_525:g.44229G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1157G>C	ENSP00000331327.5:p.Cys386Ser
ENST00000379077.9:c.*392G>C	ENSP00000368368.5:n.*392G>C
ENST00000379079.8:c.557G>C	ENSP00000368370.2:p.Cys186Ser
ENST00000448076.9:c.1208G>C	ENSP00000413452.5:p.Cys403Ser
ENST00000452863.10:c.1208G>C MANE Select	ENSP00000415516.5:p.Cys403Ser
ENST00000526685.2:n.662G>C
ENST00000639563.3:c.1157G>C	ENSP00000492269.3:p.Cys386Ser
ENST00000639907.2:n.351G>C
ENST00000640146.2:c.533G>C	ENSP00000491984.2:p.Cys178Ser
ENST00000650861.1:n.1789G>C
ENST00000651459.1:c.36-3558G>C
ENST00000651668.1:n.145G>C
ENST00000651794.1:n.951G>C
ENST00000651819.1:n.133G>C
ENST00000652579.1:n.368G>C
ENST00000652724.1:n.398G>C
ENST00000332351.7:c.1193G>C	ENSP00000331327.3:p.Cys398Ser
ENST00000379077.7:c.*392G>C	ENSP00000368368.3:n.*392G>C
ENST00000379079.6:c.557G>C	ENSP00000368370.2:p.Cys186Ser
ENST00000448076.7:c.1193G>C	ENSP00000413452.3:p.Cys398Ser
ENST00000452863.7:c.1142G>C	ENSP00000415516.3:p.Cys381Ser
ENST00000526685.1:c.20G>C	ENSP00000436292.1:p.Cys7Ser
ENST00000527882.5:c.264G>C
ENST00000530998.5:c.506G>C	ENSP00000435307.1:p.Cys169Ser
NM_000378.4:c.1142G>C	NP_000369.3:p.Cys381Ser
NM_001198551.1:c.557G>C , LRG_525t2:c.557G>C	NP_001185480.1:p.Cys186Ser
NM_001198552.1:c.506G>C	NP_001185481.1:p.Cys169Ser
NM_024424.3:c.1193G>C	NP_077742.2:p.Cys398Ser
NM_024426.4:c.1193G>C	NP_077744.3:p.Cys398Ser
NM_000378.5:c.1157G>C	NP_000369.4:p.Cys386Ser
NM_024424.4:c.1208G>C	NP_077742.3:p.Cys403Ser
NM_024426.5:c.1208G>C	NP_077744.4:p.Cys403Ser
NM_001367854.1:c.20G>C	NP_001354783.1:p.Cys7Ser
NR_160306.1:n.1540G>C
NM_000378.6:c.1157G>C	NP_000369.4:p.Cys386Ser
NM_001198552.2:c.506G>C	NP_001185481.1:p.Cys169Ser
NM_024424.5:c.1208G>C	NP_077742.3:p.Cys403Ser
NM_024426.6:c.1208G>C MANE Select	NP_077744.4:p.Cys403Ser