Canonical Allele Identifier: CA658658041

Gene: WT1

Linked Data

• ClinVar Variation Id: 476686
• ClinVar RCV Id: RCV000548802
• dbSNP Id: rs1554946803

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435332_32435333delinsAT , CM000673.2:g.32435332_32435333delinsAT	GRCh38
NC_000011.9:g.32456878_32456879delinsAT , CM000673.1:g.32456878_32456879delinsAT	GRCh37
NC_000011.8:g.32413454_32413455delinsAT	NCBI36
NG_009272.1:g.5209_5210delinsAT , LRG_525:g.5209_5210delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.28_29delinsAT	ENSP00000331327.5:p.Ala10Ile
ENST00000379077.9:c.28_29delinsAT	ENSP00000368368.5:p.Ala10Ile
ENST00000448076.9:c.28_29delinsAT	ENSP00000413452.5:p.Ala10Ile
ENST00000452863.10:c.28_29delinsAT MANE Select	ENSP00000415516.5:p.Ala10Ile
ENST00000639563.3:c.28_29delinsAT	ENSP00000492269.3:p.Ala10Ile
ENST00000332351.7:c.13_14delinsAT	ENSP00000331327.3:p.Ala5Ile
ENST00000379077.7:c.13_14delinsAT	ENSP00000368368.3:p.Ala5Ile
ENST00000448076.7:c.13_14delinsAT	ENSP00000413452.3:p.Ala5Ile
ENST00000452863.7:c.13_14delinsAT	ENSP00000415516.3:p.Ala5Ile
NM_000378.4:c.13_14delinsAT	NP_000369.3:p.Ala5Ile
NM_024424.3:c.13_14delinsAT	NP_077742.2:p.Ala5Ile
NM_024426.4:c.13_14delinsAT	NP_077744.3:p.Ala5Ile
NM_000378.5:c.28_29delinsAT	NP_000369.4:p.Ala10Ile
NM_024424.4:c.28_29delinsAT	NP_077742.3:p.Ala10Ile
NM_024426.5:c.28_29delinsAT	NP_077744.4:p.Ala10Ile
NR_160306.1:n.207_208delinsAT
NM_000378.6:c.28_29delinsAT	NP_000369.4:p.Ala10Ile
NM_024424.5:c.28_29delinsAT	NP_077742.3:p.Ala10Ile
NM_024426.6:c.28_29delinsAT MANE Select	NP_077744.4:p.Ala10Ile