Canonical Allele Identifier: CA1962323553

Gene: WT1

Linked Data

• dbSNP Id: rs1853140547

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428510_32428512del , CM000673.2:g.32428510_32428512del	GRCh38
NC_000011.9:g.32450056_32450058del , CM000673.1:g.32450056_32450058del	GRCh37
NC_000011.8:g.32406632_32406634del	NCBI36
NG_009272.1:g.12033_12035del , LRG_525:g.12033_12035del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.772_774del	ENSP00000331327.5:p.Gln258del
ENST00000379077.9:c.772_774del	ENSP00000368368.5:p.Gln258del
ENST00000379079.8:c.121_123del	ENSP00000368370.2:p.Gln41del
ENST00000448076.9:c.772_774del	ENSP00000413452.5:p.Gln258del
ENST00000452863.10:c.772_774del MANE Select	ENSP00000415516.5:p.Gln258del
ENST00000639563.3:c.772_774del	ENSP00000492269.3:p.Gln258del
ENST00000640146.2:c.148_150del	ENSP00000491984.2:p.Gln50del
ENST00000332351.7:c.757_759del	ENSP00000331327.3:p.Gln253del
ENST00000379077.7:c.757_759del	ENSP00000368368.3:p.Gln253del
ENST00000379079.6:c.121_123del	ENSP00000368370.2:p.Gln41del
ENST00000448076.7:c.757_759del	ENSP00000413452.3:p.Gln253del
ENST00000452863.7:c.757_759del	ENSP00000415516.3:p.Gln253del
ENST00000527775.1:c.10_12del	ENSP00000435351.1:p.Gln4del
ENST00000530998.5:c.121_123del	ENSP00000435307.1:p.Gln41del
NM_000378.4:c.757_759del	NP_000369.3:p.Gln253del
NM_001198551.1:c.121_123del , LRG_525t2:c.121_123del	NP_001185480.1:p.Gln41del
NM_001198552.1:c.121_123del	NP_001185481.1:p.Gln41del
NM_024424.3:c.757_759del	NP_077742.2:p.Gln253del
NM_024426.4:c.757_759del	NP_077744.3:p.Gln253del
NM_000378.5:c.772_774del	NP_000369.4:p.Gln258del
NM_024424.4:c.772_774del	NP_077742.3:p.Gln258del
NM_024426.5:c.772_774del	NP_077744.4:p.Gln258del
NR_160306.1:n.951_953del
NM_000378.6:c.772_774del	NP_000369.4:p.Gln258del
NM_001198552.2:c.121_123del	NP_001185481.1:p.Gln41del
NM_024424.5:c.772_774del	NP_077742.3:p.Gln258del
NM_024426.6:c.772_774del MANE Select	NP_077744.4:p.Gln258del