Canonical Allele Identifier: CA379965071

Gene: WT1

Linked Data

• ClinVar Variation Id: 1025295
• ClinVar RCV Id: RCV001325596
• dbSNP Id: rs1853447771
• gnomAD v4: 11-32434915-G-C
• MyVariant Identifiers: chr11:g.32456461G>C (hg19) ; chr11:g.32434915G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434915G>C , CM000673.2:g.32434915G>C	GRCh38
NC_000011.9:g.32456461G>C , CM000673.1:g.32456461G>C	GRCh37
NC_000011.8:g.32413037G>C	NCBI36
NG_009272.1:g.5627C>G , LRG_525:g.5627C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.446C>G	ENSP00000331327.5:p.Pro149Arg
ENST00000379077.9:c.446C>G	ENSP00000368368.5:p.Pro149Arg
ENST00000448076.9:c.446C>G	ENSP00000413452.5:p.Pro149Arg
ENST00000452863.10:c.446C>G MANE Select	ENSP00000415516.5:p.Pro149Arg
ENST00000639563.3:c.446C>G	ENSP00000492269.3:p.Pro149Arg
ENST00000332351.7:c.431C>G	ENSP00000331327.3:p.Pro144Arg
ENST00000379077.7:c.431C>G	ENSP00000368368.3:p.Pro144Arg
ENST00000448076.7:c.431C>G	ENSP00000413452.3:p.Pro144Arg
ENST00000452863.7:c.431C>G	ENSP00000415516.3:p.Pro144Arg
NM_000378.4:c.431C>G	NP_000369.3:p.Pro144Arg
NM_024424.3:c.431C>G	NP_077742.2:p.Pro144Arg
NM_024426.4:c.431C>G	NP_077744.3:p.Pro144Arg
NM_000378.5:c.446C>G	NP_000369.4:p.Pro149Arg
NM_024424.4:c.446C>G	NP_077742.3:p.Pro149Arg
NM_024426.5:c.446C>G	NP_077744.4:p.Pro149Arg
NR_160306.1:n.625C>G
NM_000378.6:c.446C>G	NP_000369.4:p.Pro149Arg
NM_024424.5:c.446C>G	NP_077742.3:p.Pro149Arg
NM_024426.6:c.446C>G MANE Select	NP_077744.4:p.Pro149Arg