Canonical Allele Identifier: CA473567319

Gene: WT1

Linked Data

• ClinVar Variation Id: 1101678
• ClinVar RCV Id: RCV001424697
• dbSNP Id: rs1564975679
• gnomAD v4: 11-32399972-C-T
• COSMIC: COSM926361 ; COSM1585730 ; COSM4870465
• MyVariant Identifiers: chr11:g.32421518C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399972C>T , CM000673.2:g.32399972C>T	GRCh38
NC_000011.9:g.32421518C>T , CM000673.1:g.32421518C>T	GRCh37
NC_000011.8:g.32378094C>T	NCBI36
NG_009272.1:g.40570G>A , LRG_525:g.40570G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1038G>A	ENSP00000331327.5:p.Thr346=
ENST00000379077.9:c.*273G>A	ENSP00000368368.5:n.*273G>A
ENST00000379079.8:c.438G>A	ENSP00000368370.2:p.Thr146=
ENST00000448076.9:c.1089G>A	ENSP00000413452.5:p.Thr363=
ENST00000452863.10:c.1089G>A MANE Select	ENSP00000415516.5:p.Thr363=
ENST00000526685.2:n.543G>A
ENST00000639563.3:c.1038G>A	ENSP00000492269.3:p.Thr346=
ENST00000639907.2:n.232G>A
ENST00000640146.2:c.414G>A	ENSP00000491984.2:p.Thr138=
ENST00000651459.1:c.11G>A
ENST00000651794.1:n.832G>A
ENST00000652579.1:n.249G>A
ENST00000652724.1:n.279G>A
ENST00000332351.7:c.1074G>A	ENSP00000331327.3:p.Thr358=
ENST00000379077.7:c.*273G>A	ENSP00000368368.3:n.*273G>A
ENST00000379079.6:c.438G>A	ENSP00000368370.2:p.Thr146=
ENST00000448076.7:c.1074G>A	ENSP00000413452.3:p.Thr358=
ENST00000452863.7:c.1023G>A	ENSP00000415516.3:p.Thr341=
ENST00000526685.1:c.-100G>A	ENSP00000436292.1:n.-100G>A
ENST00000527775.1:c.327G>A	ENSP00000435351.1:p.Thr109=
ENST00000527882.5:c.145G>A
ENST00000530998.5:c.387G>A	ENSP00000435307.1:p.Thr129=
NM_000378.4:c.1023G>A	NP_000369.3:p.Thr341=
NM_001198551.1:c.438G>A , LRG_525t2:c.438G>A	NP_001185480.1:p.Thr146=
NM_001198552.1:c.387G>A	NP_001185481.1:p.Thr129=
NM_024424.3:c.1074G>A	NP_077742.2:p.Thr358=
NM_024426.4:c.1074G>A	NP_077744.3:p.Thr358=
NM_000378.5:c.1038G>A	NP_000369.4:p.Thr346=
NM_024424.4:c.1089G>A	NP_077742.3:p.Thr363=
NM_024426.5:c.1089G>A	NP_077744.4:p.Thr363=
NM_001367854.1:c.-100G>A	NP_001354783.1:n.-100G>A
NR_160306.1:n.1421G>A
NM_000378.6:c.1038G>A	NP_000369.4:p.Thr346=
NM_001198552.2:c.387G>A	NP_001185481.1:p.Thr129=
NM_024424.5:c.1089G>A	NP_077742.3:p.Thr363=
NM_024426.6:c.1089G>A MANE Select	NP_077744.4:p.Thr363=