Canonical Allele Identifier: CA598392668

Gene: WT1

Linked Data

• dbSNP Id: rs1199306379
• gnomAD v2: 11-32413566-GGGA-G
• gnomAD v3: 11-32392020-GGGA-G
• gnomAD v4: 11-32392020-GGGA-G
• MyVariant Identifiers: chr11:g.32413567_32413569del (hg19) ; chr11:g.32392021_32392023del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392022_32392024del , CM000673.2:g.32392022_32392024del	GRCh38
NC_000011.9:g.32413568_32413570del , CM000673.1:g.32413568_32413570del	GRCh37
NC_000011.8:g.32370144_32370146del	NCBI36
NG_009272.1:g.48519_48521del , LRG_525:g.48519_48521del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1345_1347del	ENSP00000331327.5:p.Ser449del
ENST00000379077.9:c.*580_*582del	ENSP00000368368.5:n.*580_*582del
ENST00000379079.8:c.745_747del	ENSP00000368370.2:p.Ser249del
ENST00000448076.9:c.1396_1398del	ENSP00000413452.5:p.Ser466del
ENST00000452863.10:c.1396_1398del MANE Select	ENSP00000415516.5:p.Ser466del
ENST00000526685.2:n.850_852del
ENST00000639563.3:c.1345_1347del	ENSP00000492269.3:p.Ser449del
ENST00000639907.2:n.539_541del
ENST00000640146.2:c.721_723del	ENSP00000491984.2:p.Ser241del
ENST00000650745.1:n.1206_1208del
ENST00000650861.1:n.1977_1979del
ENST00000650986.1:n.59_61del
ENST00000651459.1:c.167_169del
ENST00000651533.1:n.442_444del
ENST00000651668.1:n.333_335del
ENST00000651794.1:n.1239_1241del
ENST00000651819.1:n.321_323del
ENST00000652579.1:n.656_658del
ENST00000652724.1:n.586_588del
ENST00000332351.7:c.1381_1383del	ENSP00000331327.3:p.Ser461del
ENST00000379077.7:c.*580_*582del	ENSP00000368368.3:n.*580_*582del
ENST00000379079.6:c.745_747del	ENSP00000368370.2:p.Ser249del
ENST00000448076.7:c.1381_1383del	ENSP00000413452.3:p.Ser461del
ENST00000452863.7:c.1330_1332del	ENSP00000415516.3:p.Ser444del
ENST00000527882.5:c.362_364del
ENST00000530998.5:c.694_696del	ENSP00000435307.1:p.Ser232del
NM_000378.4:c.1330_1332del	NP_000369.3:p.Ser444del
NM_001198551.1:c.745_747del , LRG_525t2:c.745_747del	NP_001185480.1:p.Ser249del
NM_001198552.1:c.694_696del	NP_001185481.1:p.Ser232del
NM_024424.3:c.1381_1383del	NP_077742.2:p.Ser461del
NM_024426.4:c.1381_1383del	NP_077744.3:p.Ser461del
NM_000378.5:c.1345_1347del	NP_000369.4:p.Ser449del
NM_024424.4:c.1396_1398del	NP_077742.3:p.Ser466del
NM_024426.5:c.1396_1398del	NP_077744.4:p.Ser466del
NM_001367854.1:c.208_210del	NP_001354783.1:p.Ser70del
NR_160306.1:n.1728_1730del
NM_000378.6:c.1345_1347del	NP_000369.4:p.Ser449del
NM_001198552.2:c.694_696del	NP_001185481.1:p.Ser232del
NM_024424.5:c.1396_1398del	NP_077742.3:p.Ser466del
NM_024426.6:c.1396_1398del MANE Select	NP_077744.4:p.Ser466del