Canonical Allele Identifier: CA2612986637

Gene: WT1

Linked Data

• gnomAD v4: 11-32400212-GCGAGGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400214_32400220del , CM000673.2:g.32400214_32400220del	GRCh38
NC_000011.9:g.32421760_32421766del , CM000673.1:g.32421760_32421766del	GRCh37
NC_000011.8:g.32378336_32378342del	NCBI36
NG_009272.1:g.40323_40329del , LRG_525:g.40323_40329del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.966-175_966-169del	ENSP00000331327.5:n.966-175_966-169del
ENST00000379077.9:c.*201-175_*201-169del	ENSP00000368368.5:n.*201-175_*201-169del
ENST00000379079.8:c.366-175_366-169del	ENSP00000368370.2:n.366-175_366-169del
ENST00000448076.9:c.1017-175_1017-169del	ENSP00000413452.5:n.1017-175_1017-169del
ENST00000452863.10:c.1017-175_1017-169del MANE Select	ENSP00000415516.5:n.1017-175_1017-169del
ENST00000526685.2:n.397_403del
ENST00000639563.3:c.966-175_966-169del	ENSP00000492269.3:n.966-175_966-169del
ENST00000640146.2:c.342-175_342-169del	ENSP00000491984.2:n.342-175_342-169del
ENST00000651794.1:n.760-175_760-169del
ENST00000652579.1:n.177-175_177-169del
ENST00000652724.1:n.133_139del
ENST00000332351.7:c.1002-175_1002-169del	ENSP00000331327.3:n.1002-175_1002-169del
ENST00000379077.7:c.*201-175_*201-169del	ENSP00000368368.3:n.*201-175_*201-169del
ENST00000379079.6:c.366-175_366-169del	ENSP00000368370.2:n.366-175_366-169del
ENST00000448076.7:c.1002-175_1002-169del	ENSP00000413452.3:n.1002-175_1002-169del
ENST00000452863.7:c.951-175_951-169del	ENSP00000415516.3:n.951-175_951-169del
ENST00000526685.1:c.-246_-240del	ENSP00000436292.1:n.-246_-240del
ENST00000527775.1:c.255-175_255-169del	ENSP00000435351.1:n.255-175_255-169del
ENST00000527882.5:c.73-175_73-169del
ENST00000530998.5:c.315-175_315-169del	ENSP00000435307.1:n.315-175_315-169del
NM_000378.4:c.951-175_951-169del	NP_000369.3:n.951-175_951-169del
NM_001198551.1:c.366-175_366-169del , LRG_525t2:c.366-175_366-169del	NP_001185480.1:n.366-175_366-169del
NM_001198552.1:c.315-175_315-169del	NP_001185481.1:n.315-175_315-169del
NM_024424.3:c.1002-175_1002-169del	NP_077742.2:n.1002-175_1002-169del
NM_024426.4:c.1002-175_1002-169del	NP_077744.3:n.1002-175_1002-169del
NM_000378.5:c.966-175_966-169del	NP_000369.4:n.966-175_966-169del
NM_024424.4:c.1017-175_1017-169del	NP_077742.3:n.1017-175_1017-169del
NM_024426.5:c.1017-175_1017-169del	NP_077744.4:n.1017-175_1017-169del
NM_001367854.1:c.-246_-240del	NP_001354783.1:n.-246_-240del
NR_160306.1:n.1349-175_1349-169del
NM_000378.6:c.966-175_966-169del	NP_000369.4:n.966-175_966-169del
NM_001198552.2:c.315-175_315-169del	NP_001185481.1:n.315-175_315-169del
NM_024424.5:c.1017-175_1017-169del	NP_077742.3:n.1017-175_1017-169del
NM_024426.6:c.1017-175_1017-169del MANE Select	NP_077744.4:n.1017-175_1017-169del