Canonical Allele Identifier: CA2740093683

Gene: WT1

Linked Data

• ClinVar Variation Id: 2941271
• ClinVar RCV Id: RCV003792533

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435179_32435180delinsTA , CM000673.2:g.32435179_32435180delinsTA	GRCh38
NC_000011.9:g.32456725_32456726delinsTA , CM000673.1:g.32456725_32456726delinsTA	GRCh37
NC_000011.8:g.32413301_32413302delinsTA	NCBI36
NG_009272.1:g.5362_5363delinsTA , LRG_525:g.5362_5363delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.181_182delinsTA	ENSP00000331327.5:p.Arg61Ter
ENST00000379077.9:c.181_182delinsTA	ENSP00000368368.5:p.Arg61Ter
ENST00000448076.9:c.181_182delinsTA	ENSP00000413452.5:p.Arg61Ter
ENST00000452863.10:c.181_182delinsTA MANE Select	ENSP00000415516.5:p.Arg61Ter
ENST00000639563.3:c.181_182delinsTA	ENSP00000492269.3:p.Arg61Ter
ENST00000332351.7:c.166_167delinsTA	ENSP00000331327.3:p.Arg56Ter
ENST00000379077.7:c.166_167delinsTA	ENSP00000368368.3:p.Arg56Ter
ENST00000448076.7:c.166_167delinsTA	ENSP00000413452.3:p.Arg56Ter
ENST00000452863.7:c.166_167delinsTA	ENSP00000415516.3:p.Arg56Ter
NM_000378.4:c.166_167delinsTA	NP_000369.3:p.Arg56Ter
NM_024424.3:c.166_167delinsTA	NP_077742.2:p.Arg56Ter
NM_024426.4:c.166_167delinsTA	NP_077744.3:p.Arg56Ter
NM_000378.5:c.181_182delinsTA	NP_000369.4:p.Arg61Ter
NM_024424.4:c.181_182delinsTA	NP_077742.3:p.Arg61Ter
NM_024426.5:c.181_182delinsTA	NP_077744.4:p.Arg61Ter
NR_160306.1:n.360_361delinsTA
NM_000378.6:c.181_182delinsTA	NP_000369.4:p.Arg61Ter
NM_024424.5:c.181_182delinsTA	NP_077742.3:p.Arg61Ter
NM_024426.6:c.181_182delinsTA MANE Select	NP_077744.4:p.Arg61Ter