Canonical Allele Identifier: CA379959769

Gene: WT1

Linked Data

• ClinVar Variation Id: 522401
• ClinVar RCV Id: RCV000625537
• dbSNP Id: rs1554939785
• MyVariant Identifiers: chr11:g.32417808T>G (hg19) ; chr11:g.32396262T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396262T>G , CM000673.2:g.32396262T>G	GRCh38
NC_000011.9:g.32417808T>G , CM000673.1:g.32417808T>G	GRCh37
NC_000011.8:g.32374384T>G	NCBI36
NG_009272.1:g.44280A>C , LRG_525:g.44280A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1208A>C	ENSP00000331327.5:p.His403Pro
ENST00000379077.9:c.*443A>C	ENSP00000368368.5:n.*443A>C
ENST00000379079.8:c.608A>C	ENSP00000368370.2:p.His203Pro
ENST00000448076.9:c.1259A>C	ENSP00000413452.5:p.His420Pro
ENST00000452863.10:c.1259A>C MANE Select	ENSP00000415516.5:p.His420Pro
ENST00000526685.2:n.713A>C
ENST00000639563.3:c.1208A>C	ENSP00000492269.3:p.His403Pro
ENST00000639907.2:n.402A>C
ENST00000640146.2:c.584A>C	ENSP00000491984.2:p.His195Pro
ENST00000650861.1:n.1840A>C
ENST00000651459.1:c.36-3507A>C
ENST00000651668.1:n.196A>C
ENST00000651794.1:n.1002A>C
ENST00000651819.1:n.184A>C
ENST00000652579.1:n.419A>C
ENST00000652724.1:n.449A>C
ENST00000332351.7:c.1244A>C	ENSP00000331327.3:p.His415Pro
ENST00000379077.7:c.*443A>C	ENSP00000368368.3:n.*443A>C
ENST00000379079.6:c.608A>C	ENSP00000368370.2:p.His203Pro
ENST00000448076.7:c.1244A>C	ENSP00000413452.3:p.His415Pro
ENST00000452863.7:c.1193A>C	ENSP00000415516.3:p.His398Pro
ENST00000526685.1:c.71A>C	ENSP00000436292.1:p.His24Pro
ENST00000527882.5:c.315A>C
ENST00000530998.5:c.557A>C	ENSP00000435307.1:p.His186Pro
NM_000378.4:c.1193A>C	NP_000369.3:p.His398Pro
NM_001198551.1:c.608A>C , LRG_525t2:c.608A>C	NP_001185480.1:p.His203Pro
NM_001198552.1:c.557A>C	NP_001185481.1:p.His186Pro
NM_024424.3:c.1244A>C	NP_077742.2:p.His415Pro
NM_024426.4:c.1244A>C	NP_077744.3:p.His415Pro
NM_000378.5:c.1208A>C	NP_000369.4:p.His403Pro
NM_024424.4:c.1259A>C	NP_077742.3:p.His420Pro
NM_024426.5:c.1259A>C	NP_077744.4:p.His420Pro
NM_001367854.1:c.71A>C	NP_001354783.1:p.His24Pro
NR_160306.1:n.1591A>C
NM_000378.6:c.1208A>C	NP_000369.4:p.His403Pro
NM_001198552.2:c.557A>C	NP_001185481.1:p.His186Pro
NM_024424.5:c.1259A>C	NP_077742.3:p.His420Pro
NM_024426.6:c.1259A>C MANE Select	NP_077744.4:p.His420Pro