Canonical Allele Identifier: CA1962327232

Gene: WT1

Linked Data

• ClinVar Variation Id: 1042422
• ClinVar RCV Id: RCV001346379
• dbSNP Id: rs1853451296
• gnomAD v4: 11-32434953-G-GGGTGGCGGCGGAGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434964_32434978dup , CM000673.2:g.32434964_32434978dup	GRCh38
NC_000011.9:g.32456510_32456524dup , CM000673.1:g.32456510_32456524dup	GRCh37
NC_000011.8:g.32413086_32413100dup	NCBI36
NG_009272.1:g.5574_5588dup , LRG_525:g.5574_5588dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.393_407dup	ENSP00000331327.5:p.Pro136_Pro137insAlaProProProPro
ENST00000379077.9:c.393_407dup	ENSP00000368368.5:p.Pro136_Pro137insAlaProProProPro
ENST00000448076.9:c.393_407dup	ENSP00000413452.5:p.Pro136_Pro137insAlaProProProPro
ENST00000452863.10:c.393_407dup MANE Select	ENSP00000415516.5:p.Pro136_Pro137insAlaProProProPro
ENST00000639563.3:c.393_407dup	ENSP00000492269.3:p.Pro136_Pro137insAlaProProProPro
ENST00000332351.7:c.378_392dup	ENSP00000331327.3:p.Pro131_Pro132insAlaProProProPro
ENST00000379077.7:c.378_392dup	ENSP00000368368.3:p.Pro131_Pro132insAlaProProProPro
ENST00000448076.7:c.378_392dup	ENSP00000413452.3:p.Pro131_Pro132insAlaProProProPro
ENST00000452863.7:c.378_392dup	ENSP00000415516.3:p.Pro131_Pro132insAlaProProProPro
NM_000378.4:c.378_392dup	NP_000369.3:p.Pro131_Pro132insAlaProProProPro
NM_024424.3:c.378_392dup	NP_077742.2:p.Pro131_Pro132insAlaProProProPro
NM_024426.4:c.378_392dup	NP_077744.3:p.Pro131_Pro132insAlaProProProPro
NM_000378.5:c.393_407dup	NP_000369.4:p.Pro136_Pro137insAlaProProProPro
NM_024424.4:c.393_407dup	NP_077742.3:p.Pro136_Pro137insAlaProProProPro
NM_024426.5:c.393_407dup	NP_077744.4:p.Pro136_Pro137insAlaProProProPro
NR_160306.1:n.572_586dup
NM_000378.6:c.393_407dup	NP_000369.4:p.Pro136_Pro137insAlaProProProPro
NM_024424.5:c.393_407dup	NP_077742.3:p.Pro136_Pro137insAlaProProProPro
NM_024426.6:c.393_407dup MANE Select	NP_077744.4:p.Pro136_Pro137insAlaProProProPro