Canonical Allele Identifier: CA645577451

Gene: WT1

Linked Data

• COSMIC: COSM41858

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392026_32392029dup , CM000673.2:g.32392026_32392029dup	GRCh38
NC_000011.9:g.32413572_32413575dup , CM000673.1:g.32413572_32413575dup	GRCh37
NC_000011.8:g.32370148_32370151dup	NCBI36
NG_009272.1:g.48513_48516dup , LRG_525:g.48513_48516dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1339_1342dup	ENSP00000331327.5:p.Phe448Ter
ENST00000379077.9:c.*574_*577dup	ENSP00000368368.5:n.*574_*577dup
ENST00000379079.8:c.739_742dup	ENSP00000368370.2:p.Phe248Ter
ENST00000448076.9:c.1390_1393dup	ENSP00000413452.5:p.Phe465Ter
ENST00000452863.10:c.1390_1393dup MANE Select	ENSP00000415516.5:p.Phe465Ter
ENST00000526685.2:n.844_847dup
ENST00000639563.3:c.1339_1342dup	ENSP00000492269.3:p.Phe448Ter
ENST00000639907.2:n.533_536dup
ENST00000640146.2:c.715_718dup	ENSP00000491984.2:p.Phe240Ter
ENST00000650745.1:n.1200_1203dup
ENST00000650861.1:n.1971_1974dup
ENST00000650986.1:n.53_56dup
ENST00000651459.1:c.161_164dup
ENST00000651533.1:n.436_439dup
ENST00000651668.1:n.327_330dup
ENST00000651794.1:n.1233_1236dup
ENST00000651819.1:n.315_318dup
ENST00000652579.1:n.650_653dup
ENST00000652724.1:n.580_583dup
ENST00000332351.7:c.1375_1378dup	ENSP00000331327.3:p.Phe460Ter
ENST00000379077.7:c.*574_*577dup	ENSP00000368368.3:n.*574_*577dup
ENST00000379079.6:c.739_742dup	ENSP00000368370.2:p.Phe248Ter
ENST00000448076.7:c.1375_1378dup	ENSP00000413452.3:p.Phe460Ter
ENST00000452863.7:c.1324_1327dup	ENSP00000415516.3:p.Phe443Ter
ENST00000527882.5:c.356_359dup
ENST00000530998.5:c.688_691dup	ENSP00000435307.1:p.Phe231Ter
NM_000378.4:c.1324_1327dup	NP_000369.3:p.Phe443Ter
NM_001198551.1:c.739_742dup , LRG_525t2:c.739_742dup	NP_001185480.1:p.Phe248Ter
NM_001198552.1:c.688_691dup	NP_001185481.1:p.Phe231Ter
NM_024424.3:c.1375_1378dup	NP_077742.2:p.Phe460Ter
NM_024426.4:c.1375_1378dup	NP_077744.3:p.Phe460Ter
NM_000378.5:c.1339_1342dup	NP_000369.4:p.Phe448Ter
NM_024424.4:c.1390_1393dup	NP_077742.3:p.Phe465Ter
NM_024426.5:c.1390_1393dup	NP_077744.4:p.Phe465Ter
NM_001367854.1:c.202_205dup	NP_001354783.1:p.Phe69Ter
NR_160306.1:n.1722_1725dup
NM_000378.6:c.1339_1342dup	NP_000369.4:p.Phe448Ter
NM_001198552.2:c.688_691dup	NP_001185481.1:p.Phe231Ter
NM_024424.5:c.1390_1393dup	NP_077742.3:p.Phe465Ter
NM_024426.6:c.1390_1393dup MANE Select	NP_077744.4:p.Phe465Ter