Canonical Allele Identifier: CA2612986696

Gene: WT1

Linked Data

• gnomAD v4: 11-32400263-G-GAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400264_32400265insGAA , CM000673.2:g.32400264_32400265insGAA	GRCh38
NC_000011.9:g.32421810_32421811insGAA , CM000673.1:g.32421810_32421811insGAA	GRCh37
NC_000011.8:g.32378386_32378387insGAA	NCBI36
NG_009272.1:g.40278_40279insTCT , LRG_525:g.40278_40279insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.966-220_966-219insTCT	ENSP00000331327.5:n.966-220_966-219insTCT
ENST00000379077.9:c.*201-220_*201-219insTCT	ENSP00000368368.5:n.*201-220_*201-219insTCT
ENST00000379079.8:c.366-220_366-219insTCT	ENSP00000368370.2:n.366-220_366-219insTCT
ENST00000448076.9:c.1017-220_1017-219insTCT	ENSP00000413452.5:n.1017-220_1017-219insTCT
ENST00000452863.10:c.1017-220_1017-219insTCT MANE Select	ENSP00000415516.5:n.1017-220_1017-219insTCT
ENST00000526685.2:n.352_353insTCT
ENST00000639563.3:c.966-220_966-219insTCT	ENSP00000492269.3:n.966-220_966-219insTCT
ENST00000640146.2:c.342-220_342-219insTCT	ENSP00000491984.2:n.342-220_342-219insTCT
ENST00000651794.1:n.760-220_760-219insTCT
ENST00000652579.1:n.177-220_177-219insTCT
ENST00000652724.1:n.88_89insTCT
ENST00000332351.7:c.1002-220_1002-219insTCT	ENSP00000331327.3:n.1002-220_1002-219insTCT
ENST00000379077.7:c.*201-220_*201-219insTCT	ENSP00000368368.3:n.*201-220_*201-219insTCT
ENST00000379079.6:c.366-220_366-219insTCT	ENSP00000368370.2:n.366-220_366-219insTCT
ENST00000448076.7:c.1002-220_1002-219insTCT	ENSP00000413452.3:n.1002-220_1002-219insTCT
ENST00000452863.7:c.951-220_951-219insTCT	ENSP00000415516.3:n.951-220_951-219insTCT
ENST00000526685.1:c.-291_-290insTCT	ENSP00000436292.1:n.-291_-290insTCT
ENST00000527775.1:c.255-220_255-219insTCT	ENSP00000435351.1:n.255-220_255-219insTCT
ENST00000527882.5:c.73-220_73-219insTCT
ENST00000530998.5:c.315-220_315-219insTCT	ENSP00000435307.1:n.315-220_315-219insTCT
NM_000378.4:c.951-220_951-219insTCT	NP_000369.3:n.951-220_951-219insTCT
NM_001198551.1:c.366-220_366-219insTCT , LRG_525t2:c.366-220_366-219insTCT	NP_001185480.1:n.366-220_366-219insTCT
NM_001198552.1:c.315-220_315-219insTCT	NP_001185481.1:n.315-220_315-219insTCT
NM_024424.3:c.1002-220_1002-219insTCT	NP_077742.2:n.1002-220_1002-219insTCT
NM_024426.4:c.1002-220_1002-219insTCT	NP_077744.3:n.1002-220_1002-219insTCT
NM_000378.5:c.966-220_966-219insTCT	NP_000369.4:n.966-220_966-219insTCT
NM_024424.4:c.1017-220_1017-219insTCT	NP_077742.3:n.1017-220_1017-219insTCT
NM_024426.5:c.1017-220_1017-219insTCT	NP_077744.4:n.1017-220_1017-219insTCT
NM_001367854.1:c.-291_-290insTCT	NP_001354783.1:n.-291_-290insTCT
NR_160306.1:n.1349-220_1349-219insTCT
NM_000378.6:c.966-220_966-219insTCT	NP_000369.4:n.966-220_966-219insTCT
NM_001198552.2:c.315-220_315-219insTCT	NP_001185481.1:n.315-220_315-219insTCT
NM_024424.5:c.1017-220_1017-219insTCT	NP_077742.3:n.1017-220_1017-219insTCT
NM_024426.6:c.1017-220_1017-219insTCT MANE Select	NP_077744.4:n.1017-220_1017-219insTCT