Canonical Allele Identifier: CA379958685

Gene: WT1

Linked Data

• dbSNP Id: rs2132913619
• MyVariant Identifiers: chr11:g.32413526C>G (hg19) ; chr11:g.32391980C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391980C>G , CM000673.2:g.32391980C>G	GRCh38
NC_000011.9:g.32413526C>G , CM000673.1:g.32413526C>G	GRCh37
NC_000011.8:g.32370102C>G	NCBI36
NG_009272.1:g.48562G>C , LRG_525:g.48562G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1387+1G>C	ENSP00000331327.5:n.1387+1G>C
ENST00000379077.9:c.*623G>C	ENSP00000368368.5:n.*623G>C
ENST00000379079.8:c.787+1G>C	ENSP00000368370.2:n.787+1G>C
ENST00000448076.9:c.1438+1G>C	ENSP00000413452.5:n.1438+1G>C
ENST00000452863.10:c.1439G>C MANE Select	ENSP00000415516.5:p.Gly480Ala
ENST00000526685.2:n.892+1G>C
ENST00000639563.3:c.1388G>C	ENSP00000492269.3:p.Gly463Ala
ENST00000639907.2:n.581+1G>C
ENST00000640146.2:c.764G>C	ENSP00000491984.2:p.Gly255Ala
ENST00000650745.1:n.1249G>C
ENST00000650861.1:n.2019+1G>C
ENST00000650986.1:n.102G>C
ENST00000651459.1:c.210G>C
ENST00000651533.1:n.484+1G>C
ENST00000651668.1:n.376G>C
ENST00000651794.1:n.1282G>C
ENST00000651819.1:n.364G>C
ENST00000652579.1:n.699G>C
ENST00000652724.1:n.629G>C
ENST00000332351.7:c.1424G>C	ENSP00000331327.3:p.Gly475Ala
ENST00000379077.7:c.*623G>C	ENSP00000368368.3:n.*623G>C
ENST00000379079.6:c.787+1G>C	ENSP00000368370.2:n.787+1G>C
ENST00000448076.7:c.1423+1G>C	ENSP00000413452.3:n.1423+1G>C
ENST00000452863.7:c.1372+1G>C	ENSP00000415516.3:n.1372+1G>C
ENST00000527882.5:c.405G>C
ENST00000530998.5:c.737G>C	ENSP00000435307.1:p.Gly246Ala
NM_000378.4:c.1372+1G>C	NP_000369.3:n.1372+1G>C
NM_001198551.1:c.787+1G>C , LRG_525t2:c.787+1G>C	NP_001185480.1:n.787+1G>C
NM_001198552.1:c.737G>C	NP_001185481.1:p.Gly246Ala
NM_024424.3:c.1423+1G>C	NP_077742.2:n.1423+1G>C
NM_024426.4:c.1424G>C	NP_077744.3:p.Gly475Ala
NM_000378.5:c.1387+1G>C	NP_000369.4:n.1387+1G>C
NM_024424.4:c.1438+1G>C	NP_077742.3:n.1438+1G>C
NM_024426.5:c.1439G>C	NP_077744.4:p.Gly480Ala
NM_001367854.1:c.251G>C	NP_001354783.1:p.Gly84Ala
NR_160306.1:n.1771G>C
NM_000378.6:c.1387+1G>C	NP_000369.4:n.1387+1G>C
NM_001198552.2:c.737G>C	NP_001185481.1:p.Gly246Ala
NM_024424.5:c.1438+1G>C	NP_077742.3:n.1438+1G>C
NM_024426.6:c.1439G>C MANE Select	NP_077744.4:p.Gly480Ala