Canonical Allele Identifier: CA473565478

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413609A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392063A>C , CM000673.2:g.32392063A>C	GRCh38
NC_000011.9:g.32413609A>C , CM000673.1:g.32413609A>C	GRCh37
NC_000011.8:g.32370185A>C	NCBI36
NG_009272.1:g.48479T>G , LRG_525:g.48479T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1305T>G	ENSP00000331327.5:p.Gly435=
ENST00000379077.9:c.*540T>G	ENSP00000368368.5:n.*540T>G
ENST00000379079.8:c.705T>G	ENSP00000368370.2:p.Gly235=
ENST00000448076.9:c.1356T>G	ENSP00000413452.5:p.Gly452=
ENST00000452863.10:c.1356T>G MANE Select	ENSP00000415516.5:p.Gly452=
ENST00000526685.2:n.810T>G
ENST00000639563.3:c.1305T>G	ENSP00000492269.3:p.Gly435=
ENST00000639907.2:n.499T>G
ENST00000640146.2:c.681T>G	ENSP00000491984.2:p.Gly227=
ENST00000650745.1:n.1166T>G
ENST00000650861.1:n.1937T>G
ENST00000650986.1:n.19T>G
ENST00000651459.1:c.127T>G
ENST00000651533.1:n.402T>G
ENST00000651668.1:n.293T>G
ENST00000651794.1:n.1199T>G
ENST00000651819.1:n.281T>G
ENST00000652579.1:n.616T>G
ENST00000652724.1:n.546T>G
ENST00000332351.7:c.1341T>G	ENSP00000331327.3:p.Gly447=
ENST00000379077.7:c.*540T>G	ENSP00000368368.3:n.*540T>G
ENST00000379079.6:c.705T>G	ENSP00000368370.2:p.Gly235=
ENST00000448076.7:c.1341T>G	ENSP00000413452.3:p.Gly447=
ENST00000452863.7:c.1290T>G	ENSP00000415516.3:p.Gly430=
ENST00000527882.5:c.322T>G
ENST00000530998.5:c.654T>G	ENSP00000435307.1:p.Gly218=
NM_000378.4:c.1290T>G	NP_000369.3:p.Gly430=
NM_001198551.1:c.705T>G , LRG_525t2:c.705T>G	NP_001185480.1:p.Gly235=
NM_001198552.1:c.654T>G	NP_001185481.1:p.Gly218=
NM_024424.3:c.1341T>G	NP_077742.2:p.Gly447=
NM_024426.4:c.1341T>G	NP_077744.3:p.Gly447=
NM_000378.5:c.1305T>G	NP_000369.4:p.Gly435=
NM_024424.4:c.1356T>G	NP_077742.3:p.Gly452=
NM_024426.5:c.1356T>G	NP_077744.4:p.Gly452=
NM_001367854.1:c.168T>G	NP_001354783.1:p.Gly56=
NR_160306.1:n.1688T>G
NM_000378.6:c.1305T>G	NP_000369.4:p.Gly435=
NM_001198552.2:c.654T>G	NP_001185481.1:p.Gly218=
NM_024424.5:c.1356T>G	NP_077742.3:p.Gly452=
NM_024426.6:c.1356T>G MANE Select	NP_077744.4:p.Gly452=