Canonical Allele Identifier: CA10634636

Gene: WT1

Linked Data

• ClinVar Variation Id: 304381
• ClinVar RCV Id: RCV000284238 ; RCV000339238 ; RCV000373341 ; RCV000384393
• dbSNP Id: rs58549495
• gnomAD v2: 11-32409549-AACACAC-A
• gnomAD v3: 11-32388003-AACACAC-A
• gnomAD v4: 11-32388003-AACACAC-A
• COSMIC: COSN20108127
• MyVariant Identifiers: chr11:g.32409552_32409557del (hg19) ; chr11:g.32409550_32409555del (hg19) ; chr11:g.32388006_32388011del (hg38) ; chr11:g.32388004_32388009del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32388032_32388037del , CM000673.2:g.32388032_32388037del	GRCh38
NC_000011.9:g.32409578_32409583del , CM000673.1:g.32409578_32409583del	GRCh37
NC_000011.8:g.32366154_32366159del	NCBI36
NG_009272.1:g.52533_52538del , LRG_525:g.52533_52538del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.*1049_*1054del	ENSP00000331327.5:n.*1049_*1054del
ENST00000379077.9:c.*1802_*1807del	ENSP00000368368.5:n.*1802_*1807del
ENST00000379079.8:c.*1049_*1054del	ENSP00000368370.2:n.*1049_*1054del
ENST00000452863.10:c.*1049_*1054del MANE Select	ENSP00000415516.5:n.*1049_*1054del
ENST00000651819.1:n.1543_1548del
ENST00000332351.7:c.*1049_*1054del	ENSP00000331327.3:n.*1049_*1054del
ENST00000379077.7:c.*1802_*1807del	ENSP00000368368.3:n.*1802_*1807del
ENST00000379079.6:c.*1049_*1054del	ENSP00000368370.2:n.*1049_*1054del
ENST00000452863.7:c.2543_2548del	ENSP00000415516.3:n.2543_2548del
ENST00000530998.5:c.*1049_*1054del	ENSP00000435307.1:n.*1049_*1054del
NM_000378.4:c.*1049_*1054del	NP_000369.3:n.*1049_*1054del
NM_001198551.1:c.*1049_*1054del , LRG_525t2:c.*1049_*1054del	NP_001185480.1:n.*1049_*1054del
NM_001198552.1:c.*1049_*1054del	NP_001185481.1:n.*1049_*1054del
NM_024424.3:c.*1049_*1054del	NP_077742.2:n.*1049_*1054del
NM_024426.4:c.*1049_*1054del	NP_077744.3:n.*1049_*1054del
NM_000378.5:c.*1049_*1054del	NP_000369.4:n.*1049_*1054del
NM_024424.4:c.*1049_*1054del	NP_077742.3:n.*1049_*1054del
NM_024426.5:c.*1049_*1054del	NP_077744.4:n.*1049_*1054del
NM_001367854.1:c.*1049_*1054del	NP_001354783.1:n.*1049_*1054del
NR_160306.1:n.2950_2955del
NM_000378.6:c.*1049_*1054del	NP_000369.4:n.*1049_*1054del
NM_001198552.2:c.*1049_*1054del	NP_001185481.1:n.*1049_*1054del
NM_024424.5:c.*1049_*1054del	NP_077742.3:n.*1049_*1054del
NM_024426.6:c.*1049_*1054del MANE Select	NP_077744.4:n.*1049_*1054del