Canonical Allele Identifier: CA2573146220

Gene: WT1

Linked Data

• ClinVar Variation Id: 1478819
• ClinVar RCV Id: RCV001990786
• dbSNP Id: rs2132957418

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399971_32399972delinsTT , CM000673.2:g.32399971_32399972delinsTT	GRCh38
NC_000011.9:g.32421517_32421518delinsTT , CM000673.1:g.32421517_32421518delinsTT	GRCh37
NC_000011.8:g.32378093_32378094delinsTT	NCBI36
NG_009272.1:g.40570_40571delinsAA , LRG_525:g.40570_40571delinsAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1038_1039delinsAA	ENSP00000331327.5:p.His347Asn
ENST00000379077.9:c.*273_*274delinsAA	ENSP00000368368.5:n.*273_*274delinsAA
ENST00000379079.8:c.438_439delinsAA	ENSP00000368370.2:p.His147Asn
ENST00000448076.9:c.1089_1090delinsAA	ENSP00000413452.5:p.His364Asn
ENST00000452863.10:c.1089_1090delinsAA MANE Select	ENSP00000415516.5:p.His364Asn
ENST00000526685.2:n.543_544delinsAA
ENST00000639563.3:c.1038_1039delinsAA	ENSP00000492269.3:p.His347Asn
ENST00000639907.2:n.232_233delinsAA
ENST00000640146.2:c.414_415delinsAA	ENSP00000491984.2:p.His139Asn
ENST00000651459.1:c.11_12delinsAA
ENST00000651794.1:n.832_833delinsAA
ENST00000652579.1:n.249_250delinsAA
ENST00000652724.1:n.279_280delinsAA
ENST00000332351.7:c.1074_1075delinsAA	ENSP00000331327.3:p.His359Asn
ENST00000379077.7:c.*273_*274delinsAA	ENSP00000368368.3:n.*273_*274delinsAA
ENST00000379079.6:c.438_439delinsAA	ENSP00000368370.2:p.His147Asn
ENST00000448076.7:c.1074_1075delinsAA	ENSP00000413452.3:p.His359Asn
ENST00000452863.7:c.1023_1024delinsAA	ENSP00000415516.3:p.His342Asn
ENST00000526685.1:c.-100_-99delinsAA	ENSP00000436292.1:n.-100_-99delinsAA
ENST00000527775.1:c.327_328delinsAA	ENSP00000435351.1:p.His110Asn
ENST00000527882.5:c.145_146delinsAA
ENST00000530998.5:c.387_388delinsAA	ENSP00000435307.1:p.His130Asn
NM_000378.4:c.1023_1024delinsAA	NP_000369.3:p.His342Asn
NM_001198551.1:c.438_439delinsAA , LRG_525t2:c.438_439delinsAA	NP_001185480.1:p.His147Asn
NM_001198552.1:c.387_388delinsAA	NP_001185481.1:p.His130Asn
NM_024424.3:c.1074_1075delinsAA	NP_077742.2:p.His359Asn
NM_024426.4:c.1074_1075delinsAA	NP_077744.3:p.His359Asn
NM_000378.5:c.1038_1039delinsAA	NP_000369.4:p.His347Asn
NM_024424.4:c.1089_1090delinsAA	NP_077742.3:p.His364Asn
NM_024426.5:c.1089_1090delinsAA	NP_077744.4:p.His364Asn
NM_001367854.1:c.-100_-99delinsAA	NP_001354783.1:n.-100_-99delinsAA
NR_160306.1:n.1421_1422delinsAA
NM_000378.6:c.1038_1039delinsAA	NP_000369.4:p.His347Asn
NM_001198552.2:c.387_388delinsAA	NP_001185481.1:p.His130Asn
NM_024424.5:c.1089_1090delinsAA	NP_077742.3:p.His364Asn
NM_024426.6:c.1089_1090delinsAA MANE Select	NP_077744.4:p.His364Asn