Canonical Allele Identifier: CA473565778

Gene: WT1

Linked Data

• dbSNP Id: rs2132919812
• MyVariant Identifiers: chr11:g.32414231T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392685T>C , CM000673.2:g.32392685T>C	GRCh38
NC_000011.9:g.32414231T>C , CM000673.1:g.32414231T>C	GRCh37
NC_000011.8:g.32370807T>C	NCBI36
NG_009272.1:g.47857A>G , LRG_525:g.47857A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1284A>G	ENSP00000331327.5:p.Arg428=
ENST00000379077.9:c.*519A>G	ENSP00000368368.5:n.*519A>G
ENST00000379079.8:c.684A>G	ENSP00000368370.2:p.Arg228=
ENST00000448076.9:c.1335A>G	ENSP00000413452.5:p.Arg445=
ENST00000452863.10:c.1335A>G MANE Select	ENSP00000415516.5:p.Arg445=
ENST00000526685.2:n.789A>G
ENST00000639563.3:c.1284A>G	ENSP00000492269.3:p.Arg428=
ENST00000639907.2:n.478A>G
ENST00000640146.2:c.660A>G	ENSP00000491984.2:p.Arg220=
ENST00000650745.1:n.544A>G
ENST00000650861.1:n.1916A>G
ENST00000651459.1:c.106A>G
ENST00000651533.1:n.381A>G
ENST00000651668.1:n.272A>G
ENST00000651794.1:n.1178A>G
ENST00000651819.1:n.260A>G
ENST00000652579.1:n.595A>G
ENST00000652724.1:n.525A>G
ENST00000332351.7:c.1320A>G	ENSP00000331327.3:p.Arg440=
ENST00000379077.7:c.*519A>G	ENSP00000368368.3:n.*519A>G
ENST00000379079.6:c.684A>G	ENSP00000368370.2:p.Arg228=
ENST00000448076.7:c.1320A>G	ENSP00000413452.3:p.Arg440=
ENST00000452863.7:c.1269A>G	ENSP00000415516.3:p.Arg423=
ENST00000527882.5:c.321-621A>G
ENST00000530998.5:c.633A>G	ENSP00000435307.1:p.Arg211=
NM_000378.4:c.1269A>G	NP_000369.3:p.Arg423=
NM_001198551.1:c.684A>G , LRG_525t2:c.684A>G	NP_001185480.1:p.Arg228=
NM_001198552.1:c.633A>G	NP_001185481.1:p.Arg211=
NM_024424.3:c.1320A>G	NP_077742.2:p.Arg440=
NM_024426.4:c.1320A>G	NP_077744.3:p.Arg440=
NM_000378.5:c.1284A>G	NP_000369.4:p.Arg428=
NM_024424.4:c.1335A>G	NP_077742.3:p.Arg445=
NM_024426.5:c.1335A>G	NP_077744.4:p.Arg445=
NM_001367854.1:c.147A>G	NP_001354783.1:p.Arg49=
NR_160306.1:n.1667A>G
NM_000378.6:c.1284A>G	NP_000369.4:p.Arg428=
NM_001198552.2:c.633A>G	NP_001185481.1:p.Arg211=
NM_024424.5:c.1335A>G	NP_077742.3:p.Arg445=
NM_024426.6:c.1335A>G MANE Select	NP_077744.4:p.Arg445=