Canonical Allele Identifier: CA379960333

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32421525A>C (hg19) ; chr11:g.32399979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399979A>C , CM000673.2:g.32399979A>C	GRCh38
NC_000011.9:g.32421525A>C , CM000673.1:g.32421525A>C	GRCh37
NC_000011.8:g.32378101A>C	NCBI36
NG_009272.1:g.40563T>G , LRG_525:g.40563T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1031T>G	ENSP00000331327.5:p.Ile344Arg
ENST00000379077.9:c.*266T>G	ENSP00000368368.5:n.*266T>G
ENST00000379079.8:c.431T>G	ENSP00000368370.2:p.Ile144Arg
ENST00000448076.9:c.1082T>G	ENSP00000413452.5:p.Ile361Arg
ENST00000452863.10:c.1082T>G MANE Select	ENSP00000415516.5:p.Ile361Arg
ENST00000526685.2:n.536T>G
ENST00000639563.3:c.1031T>G	ENSP00000492269.3:p.Ile344Arg
ENST00000639907.2:n.225T>G
ENST00000640146.2:c.407T>G	ENSP00000491984.2:p.Ile136Arg
ENST00000651459.1:c.4T>G
ENST00000651794.1:n.825T>G
ENST00000652579.1:n.242T>G
ENST00000652724.1:n.272T>G
ENST00000332351.7:c.1067T>G	ENSP00000331327.3:p.Ile356Arg
ENST00000379077.7:c.*266T>G	ENSP00000368368.3:n.*266T>G
ENST00000379079.6:c.431T>G	ENSP00000368370.2:p.Ile144Arg
ENST00000448076.7:c.1067T>G	ENSP00000413452.3:p.Ile356Arg
ENST00000452863.7:c.1016T>G	ENSP00000415516.3:p.Ile339Arg
ENST00000526685.1:c.-107T>G	ENSP00000436292.1:n.-107T>G
ENST00000527775.1:c.320T>G	ENSP00000435351.1:p.Ile107Arg
ENST00000527882.5:c.138T>G
ENST00000530998.5:c.380T>G	ENSP00000435307.1:p.Ile127Arg
NM_000378.4:c.1016T>G	NP_000369.3:p.Ile339Arg
NM_001198551.1:c.431T>G , LRG_525t2:c.431T>G	NP_001185480.1:p.Ile144Arg
NM_001198552.1:c.380T>G	NP_001185481.1:p.Ile127Arg
NM_024424.3:c.1067T>G	NP_077742.2:p.Ile356Arg
NM_024426.4:c.1067T>G	NP_077744.3:p.Ile356Arg
NM_000378.5:c.1031T>G	NP_000369.4:p.Ile344Arg
NM_024424.4:c.1082T>G	NP_077742.3:p.Ile361Arg
NM_024426.5:c.1082T>G	NP_077744.4:p.Ile361Arg
NM_001367854.1:c.-107T>G	NP_001354783.1:n.-107T>G
NR_160306.1:n.1414T>G
NM_000378.6:c.1031T>G	NP_000369.4:p.Ile344Arg
NM_001198552.2:c.380T>G	NP_001185481.1:p.Ile127Arg
NM_024424.5:c.1082T>G	NP_077742.3:p.Ile361Arg
NM_024426.6:c.1082T>G MANE Select	NP_077744.4:p.Ile361Arg