Canonical Allele Identifier: CA1962340668

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400131_32400132delinsGT , CM000673.2:g.32400131_32400132delinsGT	GRCh38
NC_000011.9:g.32421677_32421678delinsGT , CM000673.1:g.32421677_32421678delinsGT	GRCh37
NC_000011.8:g.32378253_32378254delinsGT	NCBI36
NG_009272.1:g.40410_40411delinsAC , LRG_525:g.40410_40411delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.966-88_966-87delinsAC	ENSP00000331327.5:n.966-88_966-87delinsAC
ENST00000379077.9:c.*201-88_*201-87delinsAC	ENSP00000368368.5:n.*201-88_*201-87delinsAC
ENST00000379079.8:c.366-88_366-87delinsAC	ENSP00000368370.2:n.366-88_366-87delinsAC
ENST00000448076.9:c.1017-88_1017-87delinsAC	ENSP00000413452.5:n.1017-88_1017-87delinsAC
ENST00000452863.10:c.1017-88_1017-87delinsAC MANE Select	ENSP00000415516.5:n.1017-88_1017-87delinsAC
ENST00000526685.2:n.470+14_470+15delinsAC
ENST00000639563.3:c.966-88_966-87delinsAC	ENSP00000492269.3:n.966-88_966-87delinsAC
ENST00000639907.2:n.72_73delinsAC
ENST00000640146.2:c.342-88_342-87delinsAC	ENSP00000491984.2:n.342-88_342-87delinsAC
ENST00000651794.1:n.760-88_760-87delinsAC
ENST00000652579.1:n.177-88_177-87delinsAC
ENST00000652724.1:n.206+14_206+15delinsAC
ENST00000332351.7:c.1002-88_1002-87delinsAC	ENSP00000331327.3:n.1002-88_1002-87delinsAC
ENST00000379077.7:c.*201-88_*201-87delinsAC	ENSP00000368368.3:n.*201-88_*201-87delinsAC
ENST00000379079.6:c.366-88_366-87delinsAC	ENSP00000368370.2:n.366-88_366-87delinsAC
ENST00000448076.7:c.1002-88_1002-87delinsAC	ENSP00000413452.3:n.1002-88_1002-87delinsAC
ENST00000452863.7:c.951-88_951-87delinsAC	ENSP00000415516.3:n.951-88_951-87delinsAC
ENST00000526685.1:c.-173+14_-173+15delinsAC	ENSP00000436292.1:n.-173+14_-173+15delinsAC
ENST00000527775.1:c.255-88_255-87delinsAC	ENSP00000435351.1:n.255-88_255-87delinsAC
ENST00000527882.5:c.73-88_73-87delinsAC
ENST00000530998.5:c.315-88_315-87delinsAC	ENSP00000435307.1:n.315-88_315-87delinsAC
NM_000378.4:c.951-88_951-87delinsAC	NP_000369.3:n.951-88_951-87delinsAC
NM_001198551.1:c.366-88_366-87delinsAC , LRG_525t2:c.366-88_366-87delinsAC	NP_001185480.1:n.366-88_366-87delinsAC
NM_001198552.1:c.315-88_315-87delinsAC	NP_001185481.1:n.315-88_315-87delinsAC
NM_024424.3:c.1002-88_1002-87delinsAC	NP_077742.2:n.1002-88_1002-87delinsAC
NM_024426.4:c.1002-88_1002-87delinsAC	NP_077744.3:n.1002-88_1002-87delinsAC
NM_000378.5:c.966-88_966-87delinsAC	NP_000369.4:n.966-88_966-87delinsAC
NM_024424.4:c.1017-88_1017-87delinsAC	NP_077742.3:n.1017-88_1017-87delinsAC
NM_024426.5:c.1017-88_1017-87delinsAC	NP_077744.4:n.1017-88_1017-87delinsAC
NM_001367854.1:c.-173+14_-173+15delinsAC	NP_001354783.1:n.-173+14_-173+15delinsAC
NR_160306.1:n.1349-88_1349-87delinsAC
NM_000378.6:c.966-88_966-87delinsAC	NP_000369.4:n.966-88_966-87delinsAC
NM_001198552.2:c.315-88_315-87delinsAC	NP_001185481.1:n.315-88_315-87delinsAC
NM_024424.5:c.1017-88_1017-87delinsAC	NP_077742.3:n.1017-88_1017-87delinsAC
NM_024426.6:c.1017-88_1017-87delinsAC MANE Select	NP_077744.4:n.1017-88_1017-87delinsAC