Canonical Allele Identifier: CA2573146230

Gene: WT1

Linked Data

• ClinVar Variation Id: 1453898
• ClinVar RCV Id: RCV001941604
• dbSNP Id: rs2133105444

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.276del	ENSP00000331327.5:p.Gly93AlafsTer9
ENST00000379077.9:c.276del	ENSP00000368368.5:p.Gly93AlafsTer9
ENST00000448076.9:c.276del	ENSP00000413452.5:p.Gly93AlafsTer9
ENST00000452863.10:c.276del MANE Select	ENSP00000415516.5:p.Gly93AlafsTer9
ENST00000639563.3:c.276del	ENSP00000492269.3:p.Gly93AlafsTer9
ENST00000332351.7:c.261del	ENSP00000331327.3:p.Gly88AlafsTer9
ENST00000379077.7:c.261del	ENSP00000368368.3:p.Gly88AlafsTer9
ENST00000448076.7:c.261del	ENSP00000413452.3:p.Gly88AlafsTer9
ENST00000452863.7:c.261del	ENSP00000415516.3:p.Gly88AlafsTer9
NM_000378.4:c.261del	NP_000369.3:p.Gly88AlafsTer9
NM_024424.3:c.261del	NP_077742.2:p.Gly88AlafsTer9
NM_024426.4:c.261del	NP_077744.3:p.Gly88AlafsTer9
NM_000378.5:c.276del	NP_000369.4:p.Gly93AlafsTer9
NM_024424.4:c.276del	NP_077742.3:p.Gly93AlafsTer9
NM_024426.5:c.276del	NP_077744.4:p.Gly93AlafsTer9
NR_160306.1:n.455del
NM_000378.6:c.276del	NP_000369.4:p.Gly93AlafsTer9
NM_024424.5:c.276del	NP_077742.3:p.Gly93AlafsTer9
NM_024426.6:c.276del MANE Select	NP_077744.4:p.Gly93AlafsTer9