Canonical Allele Identifier: CA2574790279

Gene: WT1

Linked Data

• gnomAD v4: 11-32391882-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391883_32391884del , CM000673.2:g.32391883_32391884del	GRCh38
NC_000011.9:g.32413429_32413430del , CM000673.1:g.32413429_32413430del	GRCh37
NC_000011.8:g.32370005_32370006del	NCBI36
NG_009272.1:g.48658_48659del , LRG_525:g.48658_48659del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1387+97_1387+98del	ENSP00000331327.5:n.1387+97_1387+98del
ENST00000379077.9:c.*631+88_*631+89del	ENSP00000368368.5:n.*631+88_*631+89del
ENST00000379079.8:c.787+97_787+98del	ENSP00000368370.2:n.787+97_787+98del
ENST00000448076.9:c.1438+97_1438+98del	ENSP00000413452.5:n.1438+97_1438+98del
ENST00000452863.10:c.1447+88_1447+89del MANE Select	ENSP00000415516.5:n.1447+88_1447+89del
ENST00000526685.2:n.892+97_892+98del
ENST00000639563.3:c.1396+88_1396+89del	ENSP00000492269.3:n.1396+88_1396+89del
ENST00000639907.2:n.581+97_581+98del
ENST00000640146.2:c.772+88_772+89del	ENSP00000491984.2:n.772+88_772+89del
ENST00000650745.1:n.1257+88_1257+89del
ENST00000650861.1:n.2019+97_2019+98del
ENST00000650986.1:n.110+88_110+89del
ENST00000651459.1:c.218+88_218+89del
ENST00000651533.1:n.484+97_484+98del
ENST00000651668.1:n.384+88_384+89del
ENST00000651794.1:n.1290+88_1290+89del
ENST00000651819.1:n.372+88_372+89del
ENST00000652579.1:n.707+88_707+89del
ENST00000652724.1:n.637+88_637+89del
ENST00000332351.7:c.1432+88_1432+89del	ENSP00000331327.3:n.1432+88_1432+89del
ENST00000379077.7:c.*631+88_*631+89del	ENSP00000368368.3:n.*631+88_*631+89del
ENST00000379079.6:c.787+97_787+98del	ENSP00000368370.2:n.787+97_787+98del
ENST00000448076.7:c.1423+97_1423+98del	ENSP00000413452.3:n.1423+97_1423+98del
ENST00000452863.7:c.1372+97_1372+98del	ENSP00000415516.3:n.1372+97_1372+98del
ENST00000527882.5:c.413+88_413+89del
ENST00000530998.5:c.745+88_745+89del	ENSP00000435307.1:n.745+88_745+89del
NM_000378.4:c.1372+97_1372+98del	NP_000369.3:n.1372+97_1372+98del
NM_001198551.1:c.787+97_787+98del , LRG_525t2:c.787+97_787+98del	NP_001185480.1:n.787+97_787+98del
NM_001198552.1:c.745+88_745+89del	NP_001185481.1:n.745+88_745+89del
NM_024424.3:c.1423+97_1423+98del	NP_077742.2:n.1423+97_1423+98del
NM_024426.4:c.1432+88_1432+89del	NP_077744.3:n.1432+88_1432+89del
NM_000378.5:c.1387+97_1387+98del	NP_000369.4:n.1387+97_1387+98del
NM_024424.4:c.1438+97_1438+98del	NP_077742.3:n.1438+97_1438+98del
NM_024426.5:c.1447+88_1447+89del	NP_077744.4:n.1447+88_1447+89del
NM_001367854.1:c.259+88_259+89del	NP_001354783.1:n.259+88_259+89del
NR_160306.1:n.1779+88_1779+89del
NM_000378.6:c.1387+97_1387+98del	NP_000369.4:n.1387+97_1387+98del
NM_001198552.2:c.745+88_745+89del	NP_001185481.1:n.745+88_745+89del
NM_024424.5:c.1438+97_1438+98del	NP_077742.3:n.1438+97_1438+98del
NM_024426.6:c.1447+88_1447+89del MANE Select	NP_077744.4:n.1447+88_1447+89del