Canonical Allele Identifier: CA473773290

Gene: WT1

Linked Data

• ClinVar Variation Id: 2502691
• ClinVar RCV Id: RCV003229364 ; RCV003779830
• MyVariant Identifiers: chr11:g.32456793G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435247G>C , CM000673.2:g.32435247G>C	GRCh38
NC_000011.9:g.32456793G>C , CM000673.1:g.32456793G>C	GRCh37
NC_000011.8:g.32413369G>C	NCBI36
NG_009272.1:g.5295C>G , LRG_525:g.5295C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.114C>G	ENSP00000331327.5:p.Val38=
ENST00000379077.9:c.114C>G	ENSP00000368368.5:p.Val38=
ENST00000448076.9:c.114C>G	ENSP00000413452.5:p.Val38=
ENST00000452863.10:c.114C>G MANE Select	ENSP00000415516.5:p.Val38=
ENST00000639563.3:c.114C>G	ENSP00000492269.3:p.Val38=
ENST00000332351.7:c.99C>G	ENSP00000331327.3:p.Val33=
ENST00000379077.7:c.99C>G	ENSP00000368368.3:p.Val33=
ENST00000448076.7:c.99C>G	ENSP00000413452.3:p.Val33=
ENST00000452863.7:c.99C>G	ENSP00000415516.3:p.Val33=
NM_000378.4:c.99C>G	NP_000369.3:p.Val33=
NM_024424.3:c.99C>G	NP_077742.2:p.Val33=
NM_024426.4:c.99C>G	NP_077744.3:p.Val33=
NM_000378.5:c.114C>G	NP_000369.4:p.Val38=
NM_024424.4:c.114C>G	NP_077742.3:p.Val38=
NM_024426.5:c.114C>G	NP_077744.4:p.Val38=
NR_160306.1:n.293C>G
NM_000378.6:c.114C>G	NP_000369.4:p.Val38=
NM_024424.5:c.114C>G	NP_077742.3:p.Val38=
NM_024426.6:c.114C>G MANE Select	NP_077744.4:p.Val38=