Canonical Allele Identifier: CA473565757

Gene: WT1

Linked Data

• ClinVar Variation Id: 1086595
• ClinVar RCV Id: RCV001404405
• dbSNP Id: rs1236598690
• COSMIC: COSM1722957 ; COSM1722958 ; COSM4891912
• MyVariant Identifiers: chr11:g.32414222C>T (hg19) ; chr11:g.32392676C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392676C>T , CM000673.2:g.32392676C>T	GRCh38
NC_000011.9:g.32414222C>T , CM000673.1:g.32414222C>T	GRCh37
NC_000011.8:g.32370798C>T	NCBI36
NG_009272.1:g.47866G>A , LRG_525:g.47866G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1293G>A	ENSP00000331327.5:p.Arg431=
ENST00000379077.9:c.*528G>A	ENSP00000368368.5:n.*528G>A
ENST00000379079.8:c.693G>A	ENSP00000368370.2:p.Arg231=
ENST00000448076.9:c.1344G>A	ENSP00000413452.5:p.Arg448=
ENST00000452863.10:c.1344G>A MANE Select	ENSP00000415516.5:p.Arg448=
ENST00000526685.2:n.798G>A
ENST00000639563.3:c.1293G>A	ENSP00000492269.3:p.Arg431=
ENST00000639907.2:n.487G>A
ENST00000640146.2:c.669G>A	ENSP00000491984.2:p.Arg223=
ENST00000650745.1:n.553G>A
ENST00000650861.1:n.1925G>A
ENST00000651459.1:c.115G>A
ENST00000651533.1:n.390G>A
ENST00000651668.1:n.281G>A
ENST00000651794.1:n.1187G>A
ENST00000651819.1:n.269G>A
ENST00000652579.1:n.604G>A
ENST00000652724.1:n.534G>A
ENST00000332351.7:c.1329G>A	ENSP00000331327.3:p.Arg443=
ENST00000379077.7:c.*528G>A	ENSP00000368368.3:n.*528G>A
ENST00000379079.6:c.693G>A	ENSP00000368370.2:p.Arg231=
ENST00000448076.7:c.1329G>A	ENSP00000413452.3:p.Arg443=
ENST00000452863.7:c.1278G>A	ENSP00000415516.3:p.Arg426=
ENST00000527882.5:c.321-612G>A
ENST00000530998.5:c.642G>A	ENSP00000435307.1:p.Arg214=
NM_000378.4:c.1278G>A	NP_000369.3:p.Arg426=
NM_001198551.1:c.693G>A , LRG_525t2:c.693G>A	NP_001185480.1:p.Arg231=
NM_001198552.1:c.642G>A	NP_001185481.1:p.Arg214=
NM_024424.3:c.1329G>A	NP_077742.2:p.Arg443=
NM_024426.4:c.1329G>A	NP_077744.3:p.Arg443=
NM_000378.5:c.1293G>A	NP_000369.4:p.Arg431=
NM_024424.4:c.1344G>A	NP_077742.3:p.Arg448=
NM_024426.5:c.1344G>A	NP_077744.4:p.Arg448=
NM_001367854.1:c.156G>A	NP_001354783.1:p.Arg52=
NR_160306.1:n.1676G>A
NM_000378.6:c.1293G>A	NP_000369.4:p.Arg431=
NM_001198552.2:c.642G>A	NP_001185481.1:p.Arg214=
NM_024424.5:c.1344G>A	NP_077742.3:p.Arg448=
NM_024426.6:c.1344G>A MANE Select	NP_077744.4:p.Arg448=