Canonical Allele Identifier: CA2574790574

Gene: WT1

Linked Data

• gnomAD v4: 11-32435380-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435384del , CM000673.2:g.32435384del	GRCh38
NC_000011.9:g.32456930del , CM000673.1:g.32456930del	GRCh37
NC_000011.8:g.32413506del	NCBI36
NG_009272.1:g.5161del , LRG_525:g.5161del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.-21del	ENSP00000331327.5:n.-21del
ENST00000379077.9:c.-21del	ENSP00000368368.5:n.-21del
ENST00000448076.9:c.-21del	ENSP00000413452.5:n.-21del
ENST00000452863.10:c.-21del MANE Select	ENSP00000415516.5:n.-21del
ENST00000332351.7:c.-36del	ENSP00000331327.3:n.-36del
ENST00000379077.7:c.-36del	ENSP00000368368.3:n.-36del
ENST00000448076.7:c.-36del	ENSP00000413452.3:n.-36del
NM_000378.4:c.-36del	NP_000369.3:n.-36del
NM_024424.3:c.-36del	NP_077742.2:n.-36del
NM_024426.4:c.-36del	NP_077744.3:n.-36del
NM_000378.5:c.-21del	NP_000369.4:n.-21del
NM_024424.4:c.-21del	NP_077742.3:n.-21del
NM_024426.5:c.-21del	NP_077744.4:n.-21del
NR_160306.1:n.159del
NM_000378.6:c.-21del	NP_000369.4:n.-21del
NM_024424.5:c.-21del	NP_077742.3:n.-21del
NM_024426.6:c.-21del MANE Select	NP_077744.4:n.-21del