Canonical Allele Identifier: CA2612986694

Gene: WT1

Linked Data

• gnomAD v4: 11-32400262-C-CGAGAATCGGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400264_32400265insGAATCGGAGGA , CM000673.2:g.32400264_32400265insGAATCGGAGGA	GRCh38
NC_000011.9:g.32421810_32421811insGAATCGGAGGA , CM000673.1:g.32421810_32421811insGAATCGGAGGA	GRCh37
NC_000011.8:g.32378386_32378387insGAATCGGAGGA	NCBI36
NG_009272.1:g.40279_40280insCTCCGATTCTC , LRG_525:g.40279_40280insCTCCGATTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.966-219_966-218insCTCCGATTCTC	ENSP00000331327.5:n.966-219_966-218insCTCCGATTCTC
ENST00000379077.9:c.*201-219_*201-218insCTCCGATTCTC	ENSP00000368368.5:n.*201-219_*201-218insCTCCGATTCTC
ENST00000379079.8:c.366-219_366-218insCTCCGATTCTC	ENSP00000368370.2:n.366-219_366-218insCTCCGATTCTC
ENST00000448076.9:c.1017-219_1017-218insCTCCGATTCTC	ENSP00000413452.5:n.1017-219_1017-218insCTCCGATTCTC
ENST00000452863.10:c.1017-219_1017-218insCTCCGATTCTC MANE Select	ENSP00000415516.5:n.1017-219_1017-218insCTCCGATTCTC
ENST00000526685.2:n.353_354insCTCCGATTCTC
ENST00000639563.3:c.966-219_966-218insCTCCGATTCTC	ENSP00000492269.3:n.966-219_966-218insCTCCGATTCTC
ENST00000640146.2:c.342-219_342-218insCTCCGATTCTC	ENSP00000491984.2:n.342-219_342-218insCTCCGATTCTC
ENST00000651794.1:n.760-219_760-218insCTCCGATTCTC
ENST00000652579.1:n.177-219_177-218insCTCCGATTCTC
ENST00000652724.1:n.89_90insCTCCGATTCTC
ENST00000332351.7:c.1002-219_1002-218insCTCCGATTCTC	ENSP00000331327.3:n.1002-219_1002-218insCTCCGATTCTC
ENST00000379077.7:c.*201-219_*201-218insCTCCGATTCTC	ENSP00000368368.3:n.*201-219_*201-218insCTCCGATTCTC
ENST00000379079.6:c.366-219_366-218insCTCCGATTCTC	ENSP00000368370.2:n.366-219_366-218insCTCCGATTCTC
ENST00000448076.7:c.1002-219_1002-218insCTCCGATTCTC	ENSP00000413452.3:n.1002-219_1002-218insCTCCGATTCTC
ENST00000452863.7:c.951-219_951-218insCTCCGATTCTC	ENSP00000415516.3:n.951-219_951-218insCTCCGATTCTC
ENST00000526685.1:c.-290_-289insCTCCGATTCTC	ENSP00000436292.1:n.-290_-289insCTCCGATTCTC
ENST00000527775.1:c.255-219_255-218insCTCCGATTCTC	ENSP00000435351.1:n.255-219_255-218insCTCCGATTCTC
ENST00000527882.5:c.73-219_73-218insCTCCGATTCTC
ENST00000530998.5:c.315-219_315-218insCTCCGATTCTC	ENSP00000435307.1:n.315-219_315-218insCTCCGATTCTC
NM_000378.4:c.951-219_951-218insCTCCGATTCTC	NP_000369.3:n.951-219_951-218insCTCCGATTCTC
NM_001198551.1:c.366-219_366-218insCTCCGATTCTC , LRG_525t2:c.366-219_366-218insCTCCGATTCTC	NP_001185480.1:n.366-219_366-218insCTCCGATTCTC
NM_001198552.1:c.315-219_315-218insCTCCGATTCTC	NP_001185481.1:n.315-219_315-218insCTCCGATTCTC
NM_024424.3:c.1002-219_1002-218insCTCCGATTCTC	NP_077742.2:n.1002-219_1002-218insCTCCGATTCTC
NM_024426.4:c.1002-219_1002-218insCTCCGATTCTC	NP_077744.3:n.1002-219_1002-218insCTCCGATTCTC
NM_000378.5:c.966-219_966-218insCTCCGATTCTC	NP_000369.4:n.966-219_966-218insCTCCGATTCTC
NM_024424.4:c.1017-219_1017-218insCTCCGATTCTC	NP_077742.3:n.1017-219_1017-218insCTCCGATTCTC
NM_024426.5:c.1017-219_1017-218insCTCCGATTCTC	NP_077744.4:n.1017-219_1017-218insCTCCGATTCTC
NM_001367854.1:c.-290_-289insCTCCGATTCTC	NP_001354783.1:n.-290_-289insCTCCGATTCTC
NR_160306.1:n.1349-219_1349-218insCTCCGATTCTC
NM_000378.6:c.966-219_966-218insCTCCGATTCTC	NP_000369.4:n.966-219_966-218insCTCCGATTCTC
NM_001198552.2:c.315-219_315-218insCTCCGATTCTC	NP_001185481.1:n.315-219_315-218insCTCCGATTCTC
NM_024424.5:c.1017-219_1017-218insCTCCGATTCTC	NP_077742.3:n.1017-219_1017-218insCTCCGATTCTC
NM_024426.6:c.1017-219_1017-218insCTCCGATTCTC MANE Select	NP_077744.4:n.1017-219_1017-218insCTCCGATTCTC