Canonical Allele Identifier: CA379960299

Gene: WT1

Linked Data

• dbSNP Id: rs2132957384
• MyVariant Identifiers: chr11:g.32421517G>C (hg19) ; chr11:g.32399971G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399971G>C , CM000673.2:g.32399971G>C	GRCh38
NC_000011.9:g.32421517G>C , CM000673.1:g.32421517G>C	GRCh37
NC_000011.8:g.32378093G>C	NCBI36
NG_009272.1:g.40571C>G , LRG_525:g.40571C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1039C>G	ENSP00000331327.5:p.His347Asp
ENST00000379077.9:c.*274C>G	ENSP00000368368.5:n.*274C>G
ENST00000379079.8:c.439C>G	ENSP00000368370.2:p.His147Asp
ENST00000448076.9:c.1090C>G	ENSP00000413452.5:p.His364Asp
ENST00000452863.10:c.1090C>G MANE Select	ENSP00000415516.5:p.His364Asp
ENST00000526685.2:n.544C>G
ENST00000639563.3:c.1039C>G	ENSP00000492269.3:p.His347Asp
ENST00000639907.2:n.233C>G
ENST00000640146.2:c.415C>G	ENSP00000491984.2:p.His139Asp
ENST00000651459.1:c.12C>G
ENST00000651794.1:n.833C>G
ENST00000652579.1:n.250C>G
ENST00000652724.1:n.280C>G
ENST00000332351.7:c.1075C>G	ENSP00000331327.3:p.His359Asp
ENST00000379077.7:c.*274C>G	ENSP00000368368.3:n.*274C>G
ENST00000379079.6:c.439C>G	ENSP00000368370.2:p.His147Asp
ENST00000448076.7:c.1075C>G	ENSP00000413452.3:p.His359Asp
ENST00000452863.7:c.1024C>G	ENSP00000415516.3:p.His342Asp
ENST00000526685.1:c.-99C>G	ENSP00000436292.1:n.-99C>G
ENST00000527775.1:c.328C>G	ENSP00000435351.1:p.His110Asp
ENST00000527882.5:c.146C>G
ENST00000530998.5:c.388C>G	ENSP00000435307.1:p.His130Asp
NM_000378.4:c.1024C>G	NP_000369.3:p.His342Asp
NM_001198551.1:c.439C>G , LRG_525t2:c.439C>G	NP_001185480.1:p.His147Asp
NM_001198552.1:c.388C>G	NP_001185481.1:p.His130Asp
NM_024424.3:c.1075C>G	NP_077742.2:p.His359Asp
NM_024426.4:c.1075C>G	NP_077744.3:p.His359Asp
NM_000378.5:c.1039C>G	NP_000369.4:p.His347Asp
NM_024424.4:c.1090C>G	NP_077742.3:p.His364Asp
NM_024426.5:c.1090C>G	NP_077744.4:p.His364Asp
NM_001367854.1:c.-99C>G	NP_001354783.1:n.-99C>G
NR_160306.1:n.1422C>G
NM_000378.6:c.1039C>G	NP_000369.4:p.His347Asp
NM_001198552.2:c.388C>G	NP_001185481.1:p.His130Asp
NM_024424.5:c.1090C>G	NP_077742.3:p.His364Asp
NM_024426.6:c.1090C>G MANE Select	NP_077744.4:p.His364Asp