Canonical Allele Identifier: CA936626181

Gene: WT1

Linked Data

• gnomAD v3: 11-32392019-CGGGA-C
• gnomAD v4: 11-32392019-CGGGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392021_32392024del , CM000673.2:g.32392021_32392024del	GRCh38
NC_000011.9:g.32413567_32413570del , CM000673.1:g.32413567_32413570del	GRCh37
NC_000011.8:g.32370143_32370146del	NCBI36
NG_009272.1:g.48519_48522del , LRG_525:g.48519_48522del

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1345_1348del	ENSP00000331327.5:p.Ser449GlyfsTer5
ENST00000379077.9:c.*580_*583del	ENSP00000368368.5:n.*580_*583del
ENST00000379079.8:c.745_748del	ENSP00000368370.2:p.Ser249GlyfsTer5
ENST00000448076.9:c.1396_1399del	ENSP00000413452.5:p.Ser466GlyfsTer5
ENST00000452863.10:c.1396_1399del MANE Select	ENSP00000415516.5:p.Ser466GlyfsTer5
ENST00000526685.2:n.850_853del
ENST00000639563.3:c.1345_1348del	ENSP00000492269.3:p.Ser449GlyfsTer5
ENST00000639907.2:n.539_542del
ENST00000640146.2:c.721_724del	ENSP00000491984.2:p.Ser241GlyfsTer5
ENST00000650745.1:n.1206_1209del
ENST00000650861.1:n.1977_1980del
ENST00000650986.1:n.59_62del
ENST00000651459.1:c.167_170del
ENST00000651533.1:n.442_445del
ENST00000651668.1:n.333_336del
ENST00000651794.1:n.1239_1242del
ENST00000651819.1:n.321_324del
ENST00000652579.1:n.656_659del
ENST00000652724.1:n.586_589del
ENST00000332351.7:c.1381_1384del	ENSP00000331327.3:p.Ser461GlyfsTer5
ENST00000379077.7:c.*580_*583del	ENSP00000368368.3:n.*580_*583del
ENST00000379079.6:c.745_748del	ENSP00000368370.2:p.Ser249GlyfsTer5
ENST00000448076.7:c.1381_1384del	ENSP00000413452.3:p.Ser461GlyfsTer5
ENST00000452863.7:c.1330_1333del	ENSP00000415516.3:p.Ser444GlyfsTer5
ENST00000527882.5:c.362_365del
ENST00000530998.5:c.694_697del	ENSP00000435307.1:p.Ser232GlyfsTer5
NM_000378.4:c.1330_1333del	NP_000369.3:p.Ser444GlyfsTer5
NM_001198551.1:c.745_748del , LRG_525t2:c.745_748del	NP_001185480.1:p.Ser249GlyfsTer5
NM_001198552.1:c.694_697del	NP_001185481.1:p.Ser232GlyfsTer5
NM_024424.3:c.1381_1384del	NP_077742.2:p.Ser461GlyfsTer5
NM_024426.4:c.1381_1384del	NP_077744.3:p.Ser461GlyfsTer5
NM_000378.5:c.1345_1348del	NP_000369.4:p.Ser449GlyfsTer5
NM_024424.4:c.1396_1399del	NP_077742.3:p.Ser466GlyfsTer5
NM_024426.5:c.1396_1399del	NP_077744.4:p.Ser466GlyfsTer5
NM_001367854.1:c.208_211del	NP_001354783.1:p.Ser70GlyfsTer5
NR_160306.1:n.1728_1731del
NM_000378.6:c.1345_1348del	NP_000369.4:p.Ser449GlyfsTer5
NM_001198552.2:c.694_697del	NP_001185481.1:p.Ser232GlyfsTer5
NM_024424.5:c.1396_1399del	NP_077742.3:p.Ser466GlyfsTer5
NM_024426.6:c.1396_1399del MANE Select	NP_077744.4:p.Ser466GlyfsTer5