Canonical Allele Identifier: CA379960307

Gene: WT1

Linked Data

• ClinVar Variation Id: 2198355
• ClinVar RCV Id: RCV002629325
• dbSNP Id: rs1852098454
• gnomAD v3: 11-32399973-G-T
• gnomAD v4: 11-32399973-G-T
• MyVariant Identifiers: chr11:g.32421519G>T (hg19) ; chr11:g.32399973G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399973G>T , CM000673.2:g.32399973G>T	GRCh38
NC_000011.9:g.32421519G>T , CM000673.1:g.32421519G>T	GRCh37
NC_000011.8:g.32378095G>T	NCBI36
NG_009272.1:g.40569C>A , LRG_525:g.40569C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1037C>A	ENSP00000331327.5:p.Thr346Lys
ENST00000379077.9:c.*272C>A	ENSP00000368368.5:n.*272C>A
ENST00000379079.8:c.437C>A	ENSP00000368370.2:p.Thr146Lys
ENST00000448076.9:c.1088C>A	ENSP00000413452.5:p.Thr363Lys
ENST00000452863.10:c.1088C>A MANE Select	ENSP00000415516.5:p.Thr363Lys
ENST00000526685.2:n.542C>A
ENST00000639563.3:c.1037C>A	ENSP00000492269.3:p.Thr346Lys
ENST00000639907.2:n.231C>A
ENST00000640146.2:c.413C>A	ENSP00000491984.2:p.Thr138Lys
ENST00000651459.1:c.10C>A
ENST00000651794.1:n.831C>A
ENST00000652579.1:n.248C>A
ENST00000652724.1:n.278C>A
ENST00000332351.7:c.1073C>A	ENSP00000331327.3:p.Thr358Lys
ENST00000379077.7:c.*272C>A	ENSP00000368368.3:n.*272C>A
ENST00000379079.6:c.437C>A	ENSP00000368370.2:p.Thr146Lys
ENST00000448076.7:c.1073C>A	ENSP00000413452.3:p.Thr358Lys
ENST00000452863.7:c.1022C>A	ENSP00000415516.3:p.Thr341Lys
ENST00000526685.1:c.-101C>A	ENSP00000436292.1:n.-101C>A
ENST00000527775.1:c.326C>A	ENSP00000435351.1:p.Thr109Lys
ENST00000527882.5:c.144C>A
ENST00000530998.5:c.386C>A	ENSP00000435307.1:p.Thr129Lys
NM_000378.4:c.1022C>A	NP_000369.3:p.Thr341Lys
NM_001198551.1:c.437C>A , LRG_525t2:c.437C>A	NP_001185480.1:p.Thr146Lys
NM_001198552.1:c.386C>A	NP_001185481.1:p.Thr129Lys
NM_024424.3:c.1073C>A	NP_077742.2:p.Thr358Lys
NM_024426.4:c.1073C>A	NP_077744.3:p.Thr358Lys
NM_000378.5:c.1037C>A	NP_000369.4:p.Thr346Lys
NM_024424.4:c.1088C>A	NP_077742.3:p.Thr363Lys
NM_024426.5:c.1088C>A	NP_077744.4:p.Thr363Lys
NM_001367854.1:c.-101C>A	NP_001354783.1:n.-101C>A
NR_160306.1:n.1420C>A
NM_000378.6:c.1037C>A	NP_000369.4:p.Thr346Lys
NM_001198552.2:c.386C>A	NP_001185481.1:p.Thr129Lys
NM_024424.5:c.1088C>A	NP_077742.3:p.Thr363Lys
NM_024426.6:c.1088C>A MANE Select	NP_077744.4:p.Thr363Lys