Canonical Allele Identifier: CA2573146211

Gene: WT1

Linked Data

• ClinVar Variation Id: 1467914
• ClinVar RCV Id: RCV001968739
• dbSNP Id: rs2133106703

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435209_32435210delinsTT , CM000673.2:g.32435209_32435210delinsTT	GRCh38
NC_000011.9:g.32456755_32456756delinsTT , CM000673.1:g.32456755_32456756delinsTT	GRCh37
NC_000011.8:g.32413331_32413332delinsTT	NCBI36
NG_009272.1:g.5332_5333delinsAA , LRG_525:g.5332_5333delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.151_152delinsAA	ENSP00000331327.5:p.Ala51Asn
ENST00000379077.9:c.151_152delinsAA	ENSP00000368368.5:p.Ala51Asn
ENST00000448076.9:c.151_152delinsAA	ENSP00000413452.5:p.Ala51Asn
ENST00000452863.10:c.151_152delinsAA MANE Select	ENSP00000415516.5:p.Ala51Asn
ENST00000639563.3:c.151_152delinsAA	ENSP00000492269.3:p.Ala51Asn
ENST00000332351.7:c.136_137delinsAA	ENSP00000331327.3:p.Ala46Asn
ENST00000379077.7:c.136_137delinsAA	ENSP00000368368.3:p.Ala46Asn
ENST00000448076.7:c.136_137delinsAA	ENSP00000413452.3:p.Ala46Asn
ENST00000452863.7:c.136_137delinsAA	ENSP00000415516.3:p.Ala46Asn
NM_000378.4:c.136_137delinsAA	NP_000369.3:p.Ala46Asn
NM_024424.3:c.136_137delinsAA	NP_077742.2:p.Ala46Asn
NM_024426.4:c.136_137delinsAA	NP_077744.3:p.Ala46Asn
NM_000378.5:c.151_152delinsAA	NP_000369.4:p.Ala51Asn
NM_024424.4:c.151_152delinsAA	NP_077742.3:p.Ala51Asn
NM_024426.5:c.151_152delinsAA	NP_077744.4:p.Ala51Asn
NR_160306.1:n.330_331delinsAA
NM_000378.6:c.151_152delinsAA	NP_000369.4:p.Ala51Asn
NM_024424.5:c.151_152delinsAA	NP_077742.3:p.Ala51Asn
NM_024426.6:c.151_152delinsAA MANE Select	NP_077744.4:p.Ala51Asn