Canonical Allele Identifier: CA379959867

Gene: WT1

Linked Data

• dbSNP Id: rs2132939856
• MyVariant Identifiers: chr11:g.32417848A>C (hg19) ; chr11:g.32396302A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396302A>C , CM000673.2:g.32396302A>C	GRCh38
NC_000011.9:g.32417848A>C , CM000673.1:g.32417848A>C	GRCh37
NC_000011.8:g.32374424A>C	NCBI36
NG_009272.1:g.44240T>G , LRG_525:g.44240T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1168T>G	ENSP00000331327.5:p.Tyr390Asp
ENST00000379077.9:c.*403T>G	ENSP00000368368.5:n.*403T>G
ENST00000379079.8:c.568T>G	ENSP00000368370.2:p.Tyr190Asp
ENST00000448076.9:c.1219T>G	ENSP00000413452.5:p.Tyr407Asp
ENST00000452863.10:c.1219T>G MANE Select	ENSP00000415516.5:p.Tyr407Asp
ENST00000526685.2:n.673T>G
ENST00000639563.3:c.1168T>G	ENSP00000492269.3:p.Tyr390Asp
ENST00000639907.2:n.362T>G
ENST00000640146.2:c.544T>G	ENSP00000491984.2:p.Tyr182Asp
ENST00000650861.1:n.1800T>G
ENST00000651459.1:c.36-3547T>G
ENST00000651668.1:n.156T>G
ENST00000651794.1:n.962T>G
ENST00000651819.1:n.144T>G
ENST00000652579.1:n.379T>G
ENST00000652724.1:n.409T>G
ENST00000332351.7:c.1204T>G	ENSP00000331327.3:p.Tyr402Asp
ENST00000379077.7:c.*403T>G	ENSP00000368368.3:n.*403T>G
ENST00000379079.6:c.568T>G	ENSP00000368370.2:p.Tyr190Asp
ENST00000448076.7:c.1204T>G	ENSP00000413452.3:p.Tyr402Asp
ENST00000452863.7:c.1153T>G	ENSP00000415516.3:p.Tyr385Asp
ENST00000526685.1:c.31T>G	ENSP00000436292.1:p.Tyr11Asp
ENST00000527882.5:c.275T>G
ENST00000530998.5:c.517T>G	ENSP00000435307.1:p.Tyr173Asp
NM_000378.4:c.1153T>G	NP_000369.3:p.Tyr385Asp
NM_001198551.1:c.568T>G , LRG_525t2:c.568T>G	NP_001185480.1:p.Tyr190Asp
NM_001198552.1:c.517T>G	NP_001185481.1:p.Tyr173Asp
NM_024424.3:c.1204T>G	NP_077742.2:p.Tyr402Asp
NM_024426.4:c.1204T>G	NP_077744.3:p.Tyr402Asp
NM_000378.5:c.1168T>G	NP_000369.4:p.Tyr390Asp
NM_024424.4:c.1219T>G	NP_077742.3:p.Tyr407Asp
NM_024426.5:c.1219T>G	NP_077744.4:p.Tyr407Asp
NM_001367854.1:c.31T>G	NP_001354783.1:p.Tyr11Asp
NR_160306.1:n.1551T>G
NM_000378.6:c.1168T>G	NP_000369.4:p.Tyr390Asp
NM_001198552.2:c.517T>G	NP_001185481.1:p.Tyr173Asp
NM_024424.5:c.1219T>G	NP_077742.3:p.Tyr407Asp
NM_024426.6:c.1219T>G MANE Select	NP_077744.4:p.Tyr407Asp