Canonical Allele Identifier: CA379959009

Gene: WT1

Linked Data

• dbSNP Id: rs2132915319
• MyVariant Identifiers: chr11:g.32413603T>A (hg19) ; chr11:g.32392057T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392057T>A , CM000673.2:g.32392057T>A	GRCh38
NC_000011.9:g.32413603T>A , CM000673.1:g.32413603T>A	GRCh37
NC_000011.8:g.32370179T>A	NCBI36
NG_009272.1:g.48485A>T , LRG_525:g.48485A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1311A>T	ENSP00000331327.5:p.Lys437Asn
ENST00000379077.9:c.*546A>T	ENSP00000368368.5:n.*546A>T
ENST00000379079.8:c.711A>T	ENSP00000368370.2:p.Lys237Asn
ENST00000448076.9:c.1362A>T	ENSP00000413452.5:p.Lys454Asn
ENST00000452863.10:c.1362A>T MANE Select	ENSP00000415516.5:p.Lys454Asn
ENST00000526685.2:n.816A>T
ENST00000639563.3:c.1311A>T	ENSP00000492269.3:p.Lys437Asn
ENST00000639907.2:n.505A>T
ENST00000640146.2:c.687A>T	ENSP00000491984.2:p.Lys229Asn
ENST00000650745.1:n.1172A>T
ENST00000650861.1:n.1943A>T
ENST00000650986.1:n.25A>T
ENST00000651459.1:c.133A>T
ENST00000651533.1:n.408A>T
ENST00000651668.1:n.299A>T
ENST00000651794.1:n.1205A>T
ENST00000651819.1:n.287A>T
ENST00000652579.1:n.622A>T
ENST00000652724.1:n.552A>T
ENST00000332351.7:c.1347A>T	ENSP00000331327.3:p.Lys449Asn
ENST00000379077.7:c.*546A>T	ENSP00000368368.3:n.*546A>T
ENST00000379079.6:c.711A>T	ENSP00000368370.2:p.Lys237Asn
ENST00000448076.7:c.1347A>T	ENSP00000413452.3:p.Lys449Asn
ENST00000452863.7:c.1296A>T	ENSP00000415516.3:p.Lys432Asn
ENST00000527882.5:c.328A>T
ENST00000530998.5:c.660A>T	ENSP00000435307.1:p.Lys220Asn
NM_000378.4:c.1296A>T	NP_000369.3:p.Lys432Asn
NM_001198551.1:c.711A>T , LRG_525t2:c.711A>T	NP_001185480.1:p.Lys237Asn
NM_001198552.1:c.660A>T	NP_001185481.1:p.Lys220Asn
NM_024424.3:c.1347A>T	NP_077742.2:p.Lys449Asn
NM_024426.4:c.1347A>T	NP_077744.3:p.Lys449Asn
NM_000378.5:c.1311A>T	NP_000369.4:p.Lys437Asn
NM_024424.4:c.1362A>T	NP_077742.3:p.Lys454Asn
NM_024426.5:c.1362A>T	NP_077744.4:p.Lys454Asn
NM_001367854.1:c.174A>T	NP_001354783.1:p.Lys58Asn
NR_160306.1:n.1694A>T
NM_000378.6:c.1311A>T	NP_000369.4:p.Lys437Asn
NM_001198552.2:c.660A>T	NP_001185481.1:p.Lys220Asn
NM_024424.5:c.1362A>T	NP_077742.3:p.Lys454Asn
NM_024426.6:c.1362A>T MANE Select	NP_077744.4:p.Lys454Asn