Canonical Allele Identifier: CA2612989581

Gene: WT1

Linked Data

• gnomAD v4: 11-32435082-GCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435085_32435087del , CM000673.2:g.32435085_32435087del	GRCh38
NC_000011.9:g.32456631_32456633del , CM000673.1:g.32456631_32456633del	GRCh37
NC_000011.8:g.32413207_32413209del	NCBI36
NG_009272.1:g.5457_5459del , LRG_525:g.5457_5459del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.276_278del	ENSP00000331327.5:p.Gly93del
ENST00000379077.9:c.276_278del	ENSP00000368368.5:p.Gly93del
ENST00000448076.9:c.276_278del	ENSP00000413452.5:p.Gly93del
ENST00000452863.10:c.276_278del MANE Select	ENSP00000415516.5:p.Gly93del
ENST00000639563.3:c.276_278del	ENSP00000492269.3:p.Gly93del
ENST00000332351.7:c.261_263del	ENSP00000331327.3:p.Gly88del
ENST00000379077.7:c.261_263del	ENSP00000368368.3:p.Gly88del
ENST00000448076.7:c.261_263del	ENSP00000413452.3:p.Gly88del
ENST00000452863.7:c.261_263del	ENSP00000415516.3:p.Gly88del
NM_000378.4:c.261_263del	NP_000369.3:p.Gly88del
NM_024424.3:c.261_263del	NP_077742.2:p.Gly88del
NM_024426.4:c.261_263del	NP_077744.3:p.Gly88del
NM_000378.5:c.276_278del	NP_000369.4:p.Gly93del
NM_024424.4:c.276_278del	NP_077742.3:p.Gly93del
NM_024426.5:c.276_278del	NP_077744.4:p.Gly93del
NR_160306.1:n.455_457del
NM_000378.6:c.276_278del	NP_000369.4:p.Gly93del
NM_024424.5:c.276_278del	NP_077742.3:p.Gly93del
NM_024426.6:c.276_278del MANE Select	NP_077744.4:p.Gly93del