Canonical Allele Identifier: CA2612971929

Gene: WT1

Linked Data

• gnomAD v4: 11-32388887-C-CTTCCAGGCACACCTGGTAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32388894_32388913dup , CM000673.2:g.32388894_32388913dup	GRCh38
NC_000011.9:g.32410440_32410459dup , CM000673.1:g.32410440_32410459dup	GRCh37
NC_000011.8:g.32367016_32367035dup	NCBI36
NG_009272.1:g.51635_51654dup , LRG_525:g.51635_51654dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.*151_*170dup	ENSP00000331327.5:n.*151_*170dup
ENST00000379077.9:c.*904_*923dup	ENSP00000368368.5:n.*904_*923dup
ENST00000379079.8:c.*151_*170dup	ENSP00000368370.2:n.*151_*170dup
ENST00000448076.9:c.*151_*170dup	ENSP00000413452.5:n.*151_*170dup
ENST00000452863.10:c.*151_*170dup MANE Select	ENSP00000415516.5:n.*151_*170dup
ENST00000639907.2:n.854_873dup
ENST00000640146.2:c.*151_*170dup	ENSP00000491984.2:n.*151_*170dup
ENST00000650745.1:n.1530_1549dup
ENST00000650861.1:n.2292_2311dup
ENST00000651459.1:c.491_510dup
ENST00000651533.1:n.757_776dup
ENST00000651668.1:n.657_676dup
ENST00000651794.1:n.1563_1582dup
ENST00000651819.1:n.645_664dup
ENST00000652579.1:n.980_999dup
ENST00000652724.1:n.910_929dup
ENST00000332351.7:c.*151_*170dup	ENSP00000331327.3:n.*151_*170dup
ENST00000379077.7:c.*904_*923dup	ENSP00000368368.3:n.*904_*923dup
ENST00000379079.6:c.*151_*170dup	ENSP00000368370.2:n.*151_*170dup
ENST00000448076.7:c.*151_*170dup	ENSP00000413452.3:n.*151_*170dup
ENST00000452863.7:c.1645_1664dup	ENSP00000415516.3:n.1645_1664dup
ENST00000530998.5:c.*151_*170dup	ENSP00000435307.1:n.*151_*170dup
NM_000378.4:c.*151_*170dup	NP_000369.3:n.*151_*170dup
NM_001198551.1:c.*151_*170dup , LRG_525t2:c.*151_*170dup	NP_001185480.1:n.*151_*170dup
NM_001198552.1:c.*151_*170dup	NP_001185481.1:n.*151_*170dup
NM_024424.3:c.*151_*170dup	NP_077742.2:n.*151_*170dup
NM_024426.4:c.*151_*170dup	NP_077744.3:n.*151_*170dup
NM_000378.5:c.*151_*170dup	NP_000369.4:n.*151_*170dup
NM_024424.4:c.*151_*170dup	NP_077742.3:n.*151_*170dup
NM_024426.5:c.*151_*170dup	NP_077744.4:n.*151_*170dup
NM_001367854.1:c.*151_*170dup	NP_001354783.1:n.*151_*170dup
NR_160306.1:n.2052_2071dup
NM_000378.6:c.*151_*170dup	NP_000369.4:n.*151_*170dup
NM_001198552.2:c.*151_*170dup	NP_001185481.1:n.*151_*170dup
NM_024424.5:c.*151_*170dup	NP_077742.3:n.*151_*170dup
NM_024426.6:c.*151_*170dup MANE Select	NP_077744.4:n.*151_*170dup