Canonical Allele Identifier: CA2612986654

Gene: WT1

Linked Data

• gnomAD v4: 11-32400228-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400228_32400229insAG , CM000673.2:g.32400228_32400229insAG	GRCh38
NC_000011.9:g.32421774_32421775insAG , CM000673.1:g.32421774_32421775insAG	GRCh37
NC_000011.8:g.32378350_32378351insAG	NCBI36
NG_009272.1:g.40313_40314insCT , LRG_525:g.40313_40314insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.966-185_966-184insCT	ENSP00000331327.5:n.966-185_966-184insCT
ENST00000379077.9:c.*201-185_*201-184insCT	ENSP00000368368.5:n.*201-185_*201-184insCT
ENST00000379079.8:c.366-185_366-184insCT	ENSP00000368370.2:n.366-185_366-184insCT
ENST00000448076.9:c.1017-185_1017-184insCT	ENSP00000413452.5:n.1017-185_1017-184insCT
ENST00000452863.10:c.1017-185_1017-184insCT MANE Select	ENSP00000415516.5:n.1017-185_1017-184insCT
ENST00000526685.2:n.387_388insCT
ENST00000639563.3:c.966-185_966-184insCT	ENSP00000492269.3:n.966-185_966-184insCT
ENST00000640146.2:c.342-185_342-184insCT	ENSP00000491984.2:n.342-185_342-184insCT
ENST00000651794.1:n.760-185_760-184insCT
ENST00000652579.1:n.177-185_177-184insCT
ENST00000652724.1:n.123_124insCT
ENST00000332351.7:c.1002-185_1002-184insCT	ENSP00000331327.3:n.1002-185_1002-184insCT
ENST00000379077.7:c.*201-185_*201-184insCT	ENSP00000368368.3:n.*201-185_*201-184insCT
ENST00000379079.6:c.366-185_366-184insCT	ENSP00000368370.2:n.366-185_366-184insCT
ENST00000448076.7:c.1002-185_1002-184insCT	ENSP00000413452.3:n.1002-185_1002-184insCT
ENST00000452863.7:c.951-185_951-184insCT	ENSP00000415516.3:n.951-185_951-184insCT
ENST00000526685.1:c.-256_-255insCT	ENSP00000436292.1:n.-256_-255insCT
ENST00000527775.1:c.255-185_255-184insCT	ENSP00000435351.1:n.255-185_255-184insCT
ENST00000527882.5:c.73-185_73-184insCT
ENST00000530998.5:c.315-185_315-184insCT	ENSP00000435307.1:n.315-185_315-184insCT
NM_000378.4:c.951-185_951-184insCT	NP_000369.3:n.951-185_951-184insCT
NM_001198551.1:c.366-185_366-184insCT , LRG_525t2:c.366-185_366-184insCT	NP_001185480.1:n.366-185_366-184insCT
NM_001198552.1:c.315-185_315-184insCT	NP_001185481.1:n.315-185_315-184insCT
NM_024424.3:c.1002-185_1002-184insCT	NP_077742.2:n.1002-185_1002-184insCT
NM_024426.4:c.1002-185_1002-184insCT	NP_077744.3:n.1002-185_1002-184insCT
NM_000378.5:c.966-185_966-184insCT	NP_000369.4:n.966-185_966-184insCT
NM_024424.4:c.1017-185_1017-184insCT	NP_077742.3:n.1017-185_1017-184insCT
NM_024426.5:c.1017-185_1017-184insCT	NP_077744.4:n.1017-185_1017-184insCT
NM_001367854.1:c.-256_-255insCT	NP_001354783.1:n.-256_-255insCT
NR_160306.1:n.1349-185_1349-184insCT
NM_000378.6:c.966-185_966-184insCT	NP_000369.4:n.966-185_966-184insCT
NM_001198552.2:c.315-185_315-184insCT	NP_001185481.1:n.315-185_315-184insCT
NM_024424.5:c.1017-185_1017-184insCT	NP_077742.3:n.1017-185_1017-184insCT
NM_024426.6:c.1017-185_1017-184insCT MANE Select	NP_077744.4:n.1017-185_1017-184insCT