Canonical Allele Identifier: CA379959168

Gene: WT1

Linked Data

• ClinVar Variation Id: 973193
• ClinVar RCV Id: RCV001280531 ; RCV001879755
• dbSNP Id: rs121907907
• MyVariant Identifiers: chr11:g.32414228G>T (hg19) ; chr11:g.32392682G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392682G>T , CM000673.2:g.32392682G>T	GRCh38
NC_000011.9:g.32414228G>T , CM000673.1:g.32414228G>T	GRCh37
NC_000011.8:g.32370804G>T	NCBI36
NG_009272.1:g.47860C>A , LRG_525:g.47860C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1287C>A	ENSP00000331327.5:p.His429Gln
ENST00000379077.9:c.*522C>A	ENSP00000368368.5:n.*522C>A
ENST00000379079.8:c.687C>A	ENSP00000368370.2:p.His229Gln
ENST00000448076.9:c.1338C>A	ENSP00000413452.5:p.His446Gln
ENST00000452863.10:c.1338C>A MANE Select	ENSP00000415516.5:p.His446Gln
ENST00000526685.2:n.792C>A
ENST00000639563.3:c.1287C>A	ENSP00000492269.3:p.His429Gln
ENST00000639907.2:n.481C>A
ENST00000640146.2:c.663C>A	ENSP00000491984.2:p.His221Gln
ENST00000650745.1:n.547C>A
ENST00000650861.1:n.1919C>A
ENST00000651459.1:c.109C>A
ENST00000651533.1:n.384C>A
ENST00000651668.1:n.275C>A
ENST00000651794.1:n.1181C>A
ENST00000651819.1:n.263C>A
ENST00000652579.1:n.598C>A
ENST00000652724.1:n.528C>A
ENST00000332351.7:c.1323C>A	ENSP00000331327.3:p.His441Gln
ENST00000379077.7:c.*522C>A	ENSP00000368368.3:n.*522C>A
ENST00000379079.6:c.687C>A	ENSP00000368370.2:p.His229Gln
ENST00000448076.7:c.1323C>A	ENSP00000413452.3:p.His441Gln
ENST00000452863.7:c.1272C>A	ENSP00000415516.3:p.His424Gln
ENST00000527882.5:c.321-618C>A
ENST00000530998.5:c.636C>A	ENSP00000435307.1:p.His212Gln
NM_000378.4:c.1272C>A	NP_000369.3:p.His424Gln
NM_001198551.1:c.687C>A , LRG_525t2:c.687C>A	NP_001185480.1:p.His229Gln
NM_001198552.1:c.636C>A	NP_001185481.1:p.His212Gln
NM_024424.3:c.1323C>A	NP_077742.2:p.His441Gln
NM_024426.4:c.1323C>A	NP_077744.3:p.His441Gln
NM_000378.5:c.1287C>A	NP_000369.4:p.His429Gln
NM_024424.4:c.1338C>A	NP_077742.3:p.His446Gln
NM_024426.5:c.1338C>A	NP_077744.4:p.His446Gln
NM_001367854.1:c.150C>A	NP_001354783.1:p.His50Gln
NR_160306.1:n.1670C>A
NM_000378.6:c.1287C>A	NP_000369.4:p.His429Gln
NM_001198552.2:c.636C>A	NP_001185481.1:p.His212Gln
NM_024424.5:c.1338C>A	NP_077742.3:p.His446Gln
NM_024426.6:c.1338C>A MANE Select	NP_077744.4:p.His446Gln