Canonical Allele Identifier: CA379960554

Gene: WT1

Linked Data

• dbSNP Id: rs2132959266
• MyVariant Identifiers: chr11:g.32421588T>A (hg19) ; chr11:g.32400042T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400042T>A , CM000673.2:g.32400042T>A	GRCh38
NC_000011.9:g.32421588T>A , CM000673.1:g.32421588T>A	GRCh37
NC_000011.8:g.32378164T>A	NCBI36
NG_009272.1:g.40500A>T , LRG_525:g.40500A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.968A>T	ENSP00000331327.5:p.His323Leu
ENST00000379077.9:c.*203A>T	ENSP00000368368.5:n.*203A>T
ENST00000379079.8:c.368A>T	ENSP00000368370.2:p.His123Leu
ENST00000448076.9:c.1019A>T	ENSP00000413452.5:p.His340Leu
ENST00000452863.10:c.1019A>T MANE Select	ENSP00000415516.5:p.His340Leu
ENST00000526685.2:n.473A>T
ENST00000639563.3:c.968A>T	ENSP00000492269.3:p.His323Leu
ENST00000639907.2:n.162A>T
ENST00000640146.2:c.344A>T	ENSP00000491984.2:p.His115Leu
ENST00000651794.1:n.762A>T
ENST00000652579.1:n.179A>T
ENST00000652724.1:n.209A>T
ENST00000332351.7:c.1004A>T	ENSP00000331327.3:p.His335Leu
ENST00000379077.7:c.*203A>T	ENSP00000368368.3:n.*203A>T
ENST00000379079.6:c.368A>T	ENSP00000368370.2:p.His123Leu
ENST00000448076.7:c.1004A>T	ENSP00000413452.3:p.His335Leu
ENST00000452863.7:c.953A>T	ENSP00000415516.3:p.His318Leu
ENST00000526685.1:c.-170A>T	ENSP00000436292.1:n.-170A>T
ENST00000527775.1:c.257A>T	ENSP00000435351.1:p.His86Leu
ENST00000527882.5:c.75A>T
ENST00000530998.5:c.317A>T	ENSP00000435307.1:p.His106Leu
NM_000378.4:c.953A>T	NP_000369.3:p.His318Leu
NM_001198551.1:c.368A>T , LRG_525t2:c.368A>T	NP_001185480.1:p.His123Leu
NM_001198552.1:c.317A>T	NP_001185481.1:p.His106Leu
NM_024424.3:c.1004A>T	NP_077742.2:p.His335Leu
NM_024426.4:c.1004A>T	NP_077744.3:p.His335Leu
NM_000378.5:c.968A>T	NP_000369.4:p.His323Leu
NM_024424.4:c.1019A>T	NP_077742.3:p.His340Leu
NM_024426.5:c.1019A>T	NP_077744.4:p.His340Leu
NM_001367854.1:c.-170A>T	NP_001354783.1:n.-170A>T
NR_160306.1:n.1351A>T
NM_000378.6:c.968A>T	NP_000369.4:p.His323Leu
NM_001198552.2:c.317A>T	NP_001185481.1:p.His106Leu
NM_024424.5:c.1019A>T	NP_077742.3:p.His340Leu
NM_024426.6:c.1019A>T MANE Select	NP_077744.4:p.His340Leu