Canonical Allele Identifier: CA10630786

Gene: WT1

Linked Data

• ClinVar Variation Id: 304441
• ClinVar RCV Id: RCV000266056 ; RCV000320133 ; RCV000377135
• dbSNP Id: rs886048243
• gnomAD v4: 11-32435495-C-T
• MyVariant Identifiers: chr11:g.32457041C>T (hg19) ; chr11:g.32435495C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435495C>T , CM000673.2:g.32435495C>T	GRCh38
NC_000011.9:g.32457041C>T , CM000673.1:g.32457041C>T	GRCh37
NC_000011.8:g.32413617C>T	NCBI36
NG_009272.1:g.5047G>A , LRG_525:g.5047G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.-135G>A	ENSP00000331327.5:n.-135G>A
ENST00000379077.9:c.-135G>A	ENSP00000368368.5:n.-135G>A
ENST00000448076.9:c.-135G>A	ENSP00000413452.5:n.-135G>A
ENST00000452863.10:c.-135G>A MANE Select	ENSP00000415516.5:n.-135G>A
ENST00000332351.7:c.-150G>A	ENSP00000331327.3:n.-150G>A
ENST00000448076.7:c.-150G>A	ENSP00000413452.3:n.-150G>A
NM_000378.4:c.-150G>A	NP_000369.3:n.-150G>A
NM_024424.3:c.-150G>A	NP_077742.2:n.-150G>A
NM_024426.4:c.-150G>A	NP_077744.3:n.-150G>A
NM_000378.5:c.-135G>A	NP_000369.4:n.-135G>A
NM_024424.4:c.-135G>A	NP_077742.3:n.-135G>A
NM_024426.5:c.-135G>A	NP_077744.4:n.-135G>A
NR_160306.1:n.45G>A
NM_000378.6:c.-135G>A	NP_000369.4:n.-135G>A
NM_024424.5:c.-135G>A	NP_077742.3:n.-135G>A
NM_024426.6:c.-135G>A MANE Select	NP_077744.4:n.-135G>A