Canonical Allele Identifier: CA473571619

Gene: WT1

Linked Data

• ClinVar Variation Id: 476707
• ClinVar RCV Id: RCV000536636
• dbSNP Id: rs1554946487
• MyVariant Identifiers: chr11:g.32456409A>G (hg19) ; chr11:g.32434863A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434863A>G , CM000673.2:g.32434863A>G	GRCh38
NC_000011.9:g.32456409A>G , CM000673.1:g.32456409A>G	GRCh37
NC_000011.8:g.32412985A>G	NCBI36
NG_009272.1:g.5679T>C , LRG_525:g.5679T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.498T>C	ENSP00000331327.5:p.Thr166=
ENST00000379077.9:c.498T>C	ENSP00000368368.5:p.Thr166=
ENST00000448076.9:c.498T>C	ENSP00000413452.5:p.Thr166=
ENST00000452863.10:c.498T>C MANE Select	ENSP00000415516.5:p.Thr166=
ENST00000639563.3:c.498T>C	ENSP00000492269.3:p.Thr166=
ENST00000332351.7:c.483T>C	ENSP00000331327.3:p.Thr161=
ENST00000379077.7:c.483T>C	ENSP00000368368.3:p.Thr161=
ENST00000448076.7:c.483T>C	ENSP00000413452.3:p.Thr161=
ENST00000452863.7:c.483T>C	ENSP00000415516.3:p.Thr161=
NM_000378.4:c.483T>C	NP_000369.3:p.Thr161=
NM_024424.3:c.483T>C	NP_077742.2:p.Thr161=
NM_024426.4:c.483T>C	NP_077744.3:p.Thr161=
NM_000378.5:c.498T>C	NP_000369.4:p.Thr166=
NM_024424.4:c.498T>C	NP_077742.3:p.Thr166=
NM_024426.5:c.498T>C	NP_077744.4:p.Thr166=
NR_160306.1:n.677T>C
NM_000378.6:c.498T>C	NP_000369.4:p.Thr166=
NM_024424.5:c.498T>C	NP_077742.3:p.Thr166=
NM_024426.6:c.498T>C MANE Select	NP_077744.4:p.Thr166=