Canonical Allele Identifier: CA1962333929

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32388889_32388890delinsTC , CM000673.2:g.32388889_32388890delinsTC	GRCh38
NC_000011.9:g.32410435_32410436delinsTC , CM000673.1:g.32410435_32410436delinsTC	GRCh37
NC_000011.8:g.32367011_32367012delinsTC	NCBI36
NG_009272.1:g.51652_51653delinsGA , LRG_525:g.51652_51653delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.*168_*169delinsGA	ENSP00000331327.5:n.*168_*169delinsGA
ENST00000379077.9:c.*921_*922delinsGA	ENSP00000368368.5:n.*921_*922delinsGA
ENST00000379079.8:c.*168_*169delinsGA	ENSP00000368370.2:n.*168_*169delinsGA
ENST00000448076.9:c.*168_*169delinsGA	ENSP00000413452.5:n.*168_*169delinsGA
ENST00000452863.10:c.*168_*169delinsGA MANE Select	ENSP00000415516.5:n.*168_*169delinsGA
ENST00000639907.2:n.871_872delinsGA
ENST00000640146.2:c.*168_*169delinsGA	ENSP00000491984.2:n.*168_*169delinsGA
ENST00000650745.1:n.1547_1548delinsGA
ENST00000650861.1:n.2309_2310delinsGA
ENST00000651459.1:c.508_509delinsGA
ENST00000651533.1:n.774_775delinsGA
ENST00000651668.1:n.674_675delinsGA
ENST00000651794.1:n.1580_1581delinsGA
ENST00000651819.1:n.662_663delinsGA
ENST00000652579.1:n.997_998delinsGA
ENST00000652724.1:n.927_928delinsGA
ENST00000332351.7:c.*168_*169delinsGA	ENSP00000331327.3:n.*168_*169delinsGA
ENST00000379077.7:c.*921_*922delinsGA	ENSP00000368368.3:n.*921_*922delinsGA
ENST00000379079.6:c.*168_*169delinsGA	ENSP00000368370.2:n.*168_*169delinsGA
ENST00000448076.7:c.*168_*169delinsGA	ENSP00000413452.3:n.*168_*169delinsGA
ENST00000452863.7:c.1662_1663delinsGA	ENSP00000415516.3:n.1662_1663delinsGA
ENST00000530998.5:c.*168_*169delinsGA	ENSP00000435307.1:n.*168_*169delinsGA
NM_000378.4:c.*168_*169delinsGA	NP_000369.3:n.*168_*169delinsGA
NM_001198551.1:c.*168_*169delinsGA , LRG_525t2:c.*168_*169delinsGA	NP_001185480.1:n.*168_*169delinsGA
NM_001198552.1:c.*168_*169delinsGA	NP_001185481.1:n.*168_*169delinsGA
NM_024424.3:c.*168_*169delinsGA	NP_077742.2:n.*168_*169delinsGA
NM_024426.4:c.*168_*169delinsGA	NP_077744.3:n.*168_*169delinsGA
NM_000378.5:c.*168_*169delinsGA	NP_000369.4:n.*168_*169delinsGA
NM_024424.4:c.*168_*169delinsGA	NP_077742.3:n.*168_*169delinsGA
NM_024426.5:c.*168_*169delinsGA	NP_077744.4:n.*168_*169delinsGA
NM_001367854.1:c.*168_*169delinsGA	NP_001354783.1:n.*168_*169delinsGA
NR_160306.1:n.2069_2070delinsGA
NM_000378.6:c.*168_*169delinsGA	NP_000369.4:n.*168_*169delinsGA
NM_001198552.2:c.*168_*169delinsGA	NP_001185481.1:n.*168_*169delinsGA
NM_024424.5:c.*168_*169delinsGA	NP_077742.3:n.*168_*169delinsGA
NM_024426.6:c.*168_*169delinsGA MANE Select	NP_077744.4:n.*168_*169delinsGA