Canonical Allele Identifier: CA379958682

Gene: WT1

Linked Data

• dbSNP Id: rs2132913596
• MyVariant Identifiers: chr11:g.32413525A>C (hg19) ; chr11:g.32391979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391979A>C , CM000673.2:g.32391979A>C	GRCh38
NC_000011.9:g.32413525A>C , CM000673.1:g.32413525A>C	GRCh37
NC_000011.8:g.32370101A>C	NCBI36
NG_009272.1:g.48563T>G , LRG_525:g.48563T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1387+2T>G	ENSP00000331327.5:n.1387+2T>G
ENST00000379077.9:c.*624T>G	ENSP00000368368.5:n.*624T>G
ENST00000379079.8:c.787+2T>G	ENSP00000368370.2:n.787+2T>G
ENST00000448076.9:c.1438+2T>G	ENSP00000413452.5:n.1438+2T>G
ENST00000452863.10:c.1440T>G MANE Select	ENSP00000415516.5:p.Gly480=
ENST00000526685.2:n.892+2T>G
ENST00000639563.3:c.1389T>G	ENSP00000492269.3:p.Gly463=
ENST00000639907.2:n.581+2T>G
ENST00000640146.2:c.765T>G	ENSP00000491984.2:p.Gly255=
ENST00000650745.1:n.1250T>G
ENST00000650861.1:n.2019+2T>G
ENST00000650986.1:n.103T>G
ENST00000651459.1:c.211T>G
ENST00000651533.1:n.484+2T>G
ENST00000651668.1:n.377T>G
ENST00000651794.1:n.1283T>G
ENST00000651819.1:n.365T>G
ENST00000652579.1:n.700T>G
ENST00000652724.1:n.630T>G
ENST00000332351.7:c.1425T>G	ENSP00000331327.3:p.Gly475=
ENST00000379077.7:c.*624T>G	ENSP00000368368.3:n.*624T>G
ENST00000379079.6:c.787+2T>G	ENSP00000368370.2:n.787+2T>G
ENST00000448076.7:c.1423+2T>G	ENSP00000413452.3:n.1423+2T>G
ENST00000452863.7:c.1372+2T>G	ENSP00000415516.3:n.1372+2T>G
ENST00000527882.5:c.406T>G
ENST00000530998.5:c.738T>G	ENSP00000435307.1:p.Gly246=
NM_000378.4:c.1372+2T>G	NP_000369.3:n.1372+2T>G
NM_001198551.1:c.787+2T>G , LRG_525t2:c.787+2T>G	NP_001185480.1:n.787+2T>G
NM_001198552.1:c.738T>G	NP_001185481.1:p.Gly246=
NM_024424.3:c.1423+2T>G	NP_077742.2:n.1423+2T>G
NM_024426.4:c.1425T>G	NP_077744.3:p.Gly475=
NM_000378.5:c.1387+2T>G	NP_000369.4:n.1387+2T>G
NM_024424.4:c.1438+2T>G	NP_077742.3:n.1438+2T>G
NM_024426.5:c.1440T>G	NP_077744.4:p.Gly480=
NM_001367854.1:c.252T>G	NP_001354783.1:p.Gly84=
NR_160306.1:n.1772T>G
NM_000378.6:c.1387+2T>G	NP_000369.4:n.1387+2T>G
NM_001198552.2:c.738T>G	NP_001185481.1:p.Gly246=
NM_024424.5:c.1438+2T>G	NP_077742.3:n.1438+2T>G
NM_024426.6:c.1440T>G MANE Select	NP_077744.4:p.Gly480=