Canonical Allele Identifier: CA1962340741

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400253_32400256delinsCTCA , CM000673.2:g.32400253_32400256delinsCTCA	GRCh38
NC_000011.9:g.32421799_32421802delinsCTCA , CM000673.1:g.32421799_32421802delinsCTCA	GRCh37
NC_000011.8:g.32378375_32378378delinsCTCA	NCBI36
NG_009272.1:g.40286_40289delinsTGAG , LRG_525:g.40286_40289delinsTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.966-212_966-209delinsTGAG	ENSP00000331327.5:n.966-212_966-209delinsTGAG
ENST00000379077.9:c.*201-212_*201-209delinsTGAG	ENSP00000368368.5:n.*201-212_*201-209delinsTGAG
ENST00000379079.8:c.366-212_366-209delinsTGAG	ENSP00000368370.2:n.366-212_366-209delinsTGAG
ENST00000448076.9:c.1017-212_1017-209delinsTGAG	ENSP00000413452.5:n.1017-212_1017-209delinsTGAG
ENST00000452863.10:c.1017-212_1017-209delinsTGAG MANE Select	ENSP00000415516.5:n.1017-212_1017-209delinsTGAG
ENST00000526685.2:n.360_363delinsTGAG
ENST00000639563.3:c.966-212_966-209delinsTGAG	ENSP00000492269.3:n.966-212_966-209delinsTGAG
ENST00000640146.2:c.342-212_342-209delinsTGAG	ENSP00000491984.2:n.342-212_342-209delinsTGAG
ENST00000651794.1:n.760-212_760-209delinsTGAG
ENST00000652579.1:n.177-212_177-209delinsTGAG
ENST00000652724.1:n.96_99delinsTGAG
ENST00000332351.7:c.1002-212_1002-209delinsTGAG	ENSP00000331327.3:n.1002-212_1002-209delinsTGAG
ENST00000379077.7:c.*201-212_*201-209delinsTGAG	ENSP00000368368.3:n.*201-212_*201-209delinsTGAG
ENST00000379079.6:c.366-212_366-209delinsTGAG	ENSP00000368370.2:n.366-212_366-209delinsTGAG
ENST00000448076.7:c.1002-212_1002-209delinsTGAG	ENSP00000413452.3:n.1002-212_1002-209delinsTGAG
ENST00000452863.7:c.951-212_951-209delinsTGAG	ENSP00000415516.3:n.951-212_951-209delinsTGAG
ENST00000526685.1:c.-283_-280delinsTGAG	ENSP00000436292.1:n.-283_-280delinsTGAG
ENST00000527775.1:c.255-212_255-209delinsTGAG	ENSP00000435351.1:n.255-212_255-209delinsTGAG
ENST00000527882.5:c.73-212_73-209delinsTGAG
ENST00000530998.5:c.315-212_315-209delinsTGAG	ENSP00000435307.1:n.315-212_315-209delinsTGAG
NM_000378.4:c.951-212_951-209delinsTGAG	NP_000369.3:n.951-212_951-209delinsTGAG
NM_001198551.1:c.366-212_366-209delinsTGAG , LRG_525t2:c.366-212_366-209delinsTGAG	NP_001185480.1:n.366-212_366-209delinsTGAG
NM_001198552.1:c.315-212_315-209delinsTGAG	NP_001185481.1:n.315-212_315-209delinsTGAG
NM_024424.3:c.1002-212_1002-209delinsTGAG	NP_077742.2:n.1002-212_1002-209delinsTGAG
NM_024426.4:c.1002-212_1002-209delinsTGAG	NP_077744.3:n.1002-212_1002-209delinsTGAG
NM_000378.5:c.966-212_966-209delinsTGAG	NP_000369.4:n.966-212_966-209delinsTGAG
NM_024424.4:c.1017-212_1017-209delinsTGAG	NP_077742.3:n.1017-212_1017-209delinsTGAG
NM_024426.5:c.1017-212_1017-209delinsTGAG	NP_077744.4:n.1017-212_1017-209delinsTGAG
NM_001367854.1:c.-283_-280delinsTGAG	NP_001354783.1:n.-283_-280delinsTGAG
NR_160306.1:n.1349-212_1349-209delinsTGAG
NM_000378.6:c.966-212_966-209delinsTGAG	NP_000369.4:n.966-212_966-209delinsTGAG
NM_001198552.2:c.315-212_315-209delinsTGAG	NP_001185481.1:n.315-212_315-209delinsTGAG
NM_024424.5:c.1017-212_1017-209delinsTGAG	NP_077742.3:n.1017-212_1017-209delinsTGAG
NM_024426.6:c.1017-212_1017-209delinsTGAG MANE Select	NP_077744.4:n.1017-212_1017-209delinsTGAG