Canonical Allele Identifier: CA064226

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396416A>G , CM000673.2:g.32396416A>G	GRCh38
NC_000011.9:g.32417962A>G , CM000673.1:g.32417962A>G	GRCh37
NC_000011.8:g.32374538A>G	NCBI36
NG_009272.1:g.44126T>C , LRG_525:g.44126T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1063-9T>C	ENSP00000331327.5:n.1063-9T>C
ENST00000379077.9:c.*298-9T>C	ENSP00000368368.5:n.*298-9T>C
ENST00000379079.8:c.463-9T>C	ENSP00000368370.2:n.463-9T>C
ENST00000448076.9:c.1114-9T>C	ENSP00000413452.5:n.1114-9T>C
ENST00000452863.10:c.1114-9T>C MANE Select	ENSP00000415516.5:n.1114-9T>C
ENST00000526685.2:n.568-9T>C
ENST00000639563.3:c.1063-9T>C	ENSP00000492269.3:n.1063-9T>C
ENST00000639907.2:n.257-9T>C
ENST00000640146.2:c.439-9T>C	ENSP00000491984.2:n.439-9T>C
ENST00000650861.1:n.1686T>C
ENST00000651459.1:c.35+3532T>C
ENST00000651668.1:n.51-9T>C
ENST00000651794.1:n.857-9T>C
ENST00000651819.1:n.30T>C
ENST00000652579.1:n.274-9T>C
ENST00000652724.1:n.304-9T>C
ENST00000332351.7:c.1099-9T>C	ENSP00000331327.3:n.1099-9T>C
ENST00000379077.7:c.*298-9T>C	ENSP00000368368.3:n.*298-9T>C
ENST00000379079.6:c.463-9T>C	ENSP00000368370.2:n.463-9T>C
ENST00000448076.7:c.1099-9T>C	ENSP00000413452.3:n.1099-9T>C
ENST00000452863.7:c.1048-9T>C	ENSP00000415516.3:n.1048-9T>C
ENST00000526685.1:c.-75-9T>C	ENSP00000436292.1:n.-75-9T>C
ENST00000527775.1:c.352-9T>C	ENSP00000435351.1:n.352-9T>C
ENST00000527882.5:c.170-9T>C
ENST00000530998.5:c.412-9T>C	ENSP00000435307.1:n.412-9T>C
NM_000378.4:c.1048-9T>C	NP_000369.3:n.1048-9T>C
NM_001198551.1:c.463-9T>C , LRG_525t2:c.463-9T>C	NP_001185480.1:n.463-9T>C
NM_001198552.1:c.412-9T>C	NP_001185481.1:n.412-9T>C
NM_024424.3:c.1099-9T>C	NP_077742.2:n.1099-9T>C
NM_024426.4:c.1099-9T>C	NP_077744.3:n.1099-9T>C
NM_000378.5:c.1063-9T>C	NP_000369.4:n.1063-9T>C
NM_024424.4:c.1114-9T>C	NP_077742.3:n.1114-9T>C
NM_024426.5:c.1114-9T>C	NP_077744.4:n.1114-9T>C
NM_001367854.1:c.-75-9T>C	NP_001354783.1:n.-75-9T>C
NR_160306.1:n.1446-9T>C
NM_000378.6:c.1063-9T>C	NP_000369.4:n.1063-9T>C
NM_001198552.2:c.412-9T>C	NP_001185481.1:n.412-9T>C
NM_024424.5:c.1114-9T>C	NP_077742.3:n.1114-9T>C
NM_024426.6:c.1114-9T>C MANE Select	NP_077744.4:n.1114-9T>C