Canonical Allele Identifier: CA473565785

Gene: WT1

Linked Data

• ClinVar Variation Id: 1107007
• ClinVar RCV Id: RCV001431979
• dbSNP Id: rs1319380075
• gnomAD v2: 11-32414234-T-C
• gnomAD v4: 11-32392688-T-C
• MyVariant Identifiers: chr11:g.32414234T>C (hg19) ; chr11:g.32392688T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392688T>C , CM000673.2:g.32392688T>C	GRCh38
NC_000011.9:g.32414234T>C , CM000673.1:g.32414234T>C	GRCh37
NC_000011.8:g.32370810T>C	NCBI36
NG_009272.1:g.47854A>G , LRG_525:g.47854A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1281A>G	ENSP00000331327.5:p.Lys427=
ENST00000379077.9:c.*516A>G	ENSP00000368368.5:n.*516A>G
ENST00000379079.8:c.681A>G	ENSP00000368370.2:p.Lys227=
ENST00000448076.9:c.1332A>G	ENSP00000413452.5:p.Lys444=
ENST00000452863.10:c.1332A>G MANE Select	ENSP00000415516.5:p.Lys444=
ENST00000526685.2:n.786A>G
ENST00000639563.3:c.1281A>G	ENSP00000492269.3:p.Lys427=
ENST00000639907.2:n.475A>G
ENST00000640146.2:c.657A>G	ENSP00000491984.2:p.Lys219=
ENST00000650745.1:n.541A>G
ENST00000650861.1:n.1913A>G
ENST00000651459.1:c.103A>G
ENST00000651533.1:n.378A>G
ENST00000651668.1:n.269A>G
ENST00000651794.1:n.1175A>G
ENST00000651819.1:n.257A>G
ENST00000652579.1:n.592A>G
ENST00000652724.1:n.522A>G
ENST00000332351.7:c.1317A>G	ENSP00000331327.3:p.Lys439=
ENST00000379077.7:c.*516A>G	ENSP00000368368.3:n.*516A>G
ENST00000379079.6:c.681A>G	ENSP00000368370.2:p.Lys227=
ENST00000448076.7:c.1317A>G	ENSP00000413452.3:p.Lys439=
ENST00000452863.7:c.1266A>G	ENSP00000415516.3:p.Lys422=
ENST00000527882.5:c.321-624A>G
ENST00000530998.5:c.630A>G	ENSP00000435307.1:p.Lys210=
NM_000378.4:c.1266A>G	NP_000369.3:p.Lys422=
NM_001198551.1:c.681A>G , LRG_525t2:c.681A>G	NP_001185480.1:p.Lys227=
NM_001198552.1:c.630A>G	NP_001185481.1:p.Lys210=
NM_024424.3:c.1317A>G	NP_077742.2:p.Lys439=
NM_024426.4:c.1317A>G	NP_077744.3:p.Lys439=
NM_000378.5:c.1281A>G	NP_000369.4:p.Lys427=
NM_024424.4:c.1332A>G	NP_077742.3:p.Lys444=
NM_024426.5:c.1332A>G	NP_077744.4:p.Lys444=
NM_001367854.1:c.144A>G	NP_001354783.1:p.Lys48=
NR_160306.1:n.1664A>G
NM_000378.6:c.1281A>G	NP_000369.4:p.Lys427=
NM_001198552.2:c.630A>G	NP_001185481.1:p.Lys210=
NM_024424.5:c.1332A>G	NP_077742.3:p.Lys444=
NM_024426.6:c.1332A>G MANE Select	NP_077744.4:p.Lys444=