Canonical Allele Identifier: CA473568318

Gene: WT1

Linked Data

• COSMIC: COSM21541
• MyVariant Identifiers: chr11:g.32439158del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417613del , CM000673.2:g.32417613del	GRCh38
NC_000011.9:g.32439159del , CM000673.1:g.32439159del	GRCh37
NC_000011.8:g.32395735del	NCBI36
NG_009272.1:g.22930del , LRG_525:g.22930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.930del	ENSP00000331327.5:p.Trp311GlyfsTer4
ENST00000379077.9:c.930del	ENSP00000368368.5:p.Trp311GlyfsTer4
ENST00000379079.8:c.279del	ENSP00000368370.2:p.Trp94GlyfsTer4
ENST00000448076.9:c.930del	ENSP00000413452.5:p.Trp311GlyfsTer4
ENST00000452863.10:c.930del MANE Select	ENSP00000415516.5:p.Trp311GlyfsTer4
ENST00000639563.3:c.930del	ENSP00000492269.3:p.Trp311GlyfsTer4
ENST00000640146.2:c.306del	ENSP00000491984.2:p.Trp103GlyfsTer4
ENST00000332351.7:c.915del	ENSP00000331327.3:p.Trp306GlyfsTer4
ENST00000379077.7:c.915del	ENSP00000368368.3:p.Trp306GlyfsTer4
ENST00000379079.6:c.279del	ENSP00000368370.2:p.Trp94GlyfsTer4
ENST00000448076.7:c.915del	ENSP00000413452.3:p.Trp306GlyfsTer4
ENST00000452863.7:c.915del	ENSP00000415516.3:p.Trp306GlyfsTer4
ENST00000527775.1:c.168del	ENSP00000435351.1:p.Trp57GlyfsTer4
ENST00000530998.5:c.279del	ENSP00000435307.1:p.Trp94GlyfsTer4
NM_000378.4:c.915del	NP_000369.3:p.Trp306GlyfsTer4
NM_001198551.1:c.279del , LRG_525t2:c.279del	NP_001185480.1:p.Trp94GlyfsTer4
NM_001198552.1:c.279del	NP_001185481.1:p.Trp94GlyfsTer4
NM_024424.3:c.915del	NP_077742.2:p.Trp306GlyfsTer4
NM_024426.4:c.915del	NP_077744.3:p.Trp306GlyfsTer4
NM_000378.5:c.930del	NP_000369.4:p.Trp311GlyfsTer4
NM_024424.4:c.930del	NP_077742.3:p.Trp311GlyfsTer4
NM_024426.5:c.930del	NP_077744.4:p.Trp311GlyfsTer4
NR_160306.1:n.1109del
NM_000378.6:c.930del	NP_000369.4:p.Trp311GlyfsTer4
NM_001198552.2:c.279del	NP_001185481.1:p.Trp94GlyfsTer4
NM_024424.5:c.930del	NP_077742.3:p.Trp311GlyfsTer4
NM_024426.6:c.930del MANE Select	NP_077744.4:p.Trp311GlyfsTer4