Canonical Allele Identifier: CA379960424

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32421550T>G (hg19) ; chr11:g.32400004T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400004T>G , CM000673.2:g.32400004T>G	GRCh38
NC_000011.9:g.32421550T>G , CM000673.1:g.32421550T>G	GRCh37
NC_000011.8:g.32378126T>G	NCBI36
NG_009272.1:g.40538A>C , LRG_525:g.40538A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1006A>C	ENSP00000331327.5:p.Ile336Leu
ENST00000379077.9:c.*241A>C	ENSP00000368368.5:n.*241A>C
ENST00000379079.8:c.406A>C	ENSP00000368370.2:p.Ile136Leu
ENST00000448076.9:c.1057A>C	ENSP00000413452.5:p.Ile353Leu
ENST00000452863.10:c.1057A>C MANE Select	ENSP00000415516.5:p.Ile353Leu
ENST00000526685.2:n.511A>C
ENST00000639563.3:c.1006A>C	ENSP00000492269.3:p.Ile336Leu
ENST00000639907.2:n.200A>C
ENST00000640146.2:c.382A>C	ENSP00000491984.2:p.Ile128Leu
ENST00000651794.1:n.800A>C
ENST00000652579.1:n.217A>C
ENST00000652724.1:n.247A>C
ENST00000332351.7:c.1042A>C	ENSP00000331327.3:p.Ile348Leu
ENST00000379077.7:c.*241A>C	ENSP00000368368.3:n.*241A>C
ENST00000379079.6:c.406A>C	ENSP00000368370.2:p.Ile136Leu
ENST00000448076.7:c.1042A>C	ENSP00000413452.3:p.Ile348Leu
ENST00000452863.7:c.991A>C	ENSP00000415516.3:p.Ile331Leu
ENST00000526685.1:c.-132A>C	ENSP00000436292.1:n.-132A>C
ENST00000527775.1:c.295A>C	ENSP00000435351.1:p.Ile99Leu
ENST00000527882.5:c.113A>C
ENST00000530998.5:c.355A>C	ENSP00000435307.1:p.Ile119Leu
NM_000378.4:c.991A>C	NP_000369.3:p.Ile331Leu
NM_001198551.1:c.406A>C , LRG_525t2:c.406A>C	NP_001185480.1:p.Ile136Leu
NM_001198552.1:c.355A>C	NP_001185481.1:p.Ile119Leu
NM_024424.3:c.1042A>C	NP_077742.2:p.Ile348Leu
NM_024426.4:c.1042A>C	NP_077744.3:p.Ile348Leu
NM_000378.5:c.1006A>C	NP_000369.4:p.Ile336Leu
NM_024424.4:c.1057A>C	NP_077742.3:p.Ile353Leu
NM_024426.5:c.1057A>C	NP_077744.4:p.Ile353Leu
NM_001367854.1:c.-132A>C	NP_001354783.1:n.-132A>C
NR_160306.1:n.1389A>C
NM_000378.6:c.1006A>C	NP_000369.4:p.Ile336Leu
NM_001198552.2:c.355A>C	NP_001185481.1:p.Ile119Leu
NM_024424.5:c.1057A>C	NP_077742.3:p.Ile353Leu
NM_024426.6:c.1057A>C MANE Select	NP_077744.4:p.Ile353Leu