Canonical Allele Identifier: CA2695201111

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428046_32428047dup , CM000673.2:g.32428046_32428047dup	GRCh38
NC_000011.9:g.32449592_32449593dup , CM000673.1:g.32449592_32449593dup	GRCh37
NC_000011.8:g.32406168_32406169dup	NCBI36
NG_009272.1:g.12495_12496dup , LRG_525:g.12495_12496dup

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.796_797dup MANE Select	NP_077744.4:p.Ser267ThrfsTer25
ENST00000452863.10:c.796_797dup MANE Select	ENSP00000415516.5:p.Ser267ThrfsTer25
NM_000378.4:c.781_782dup	NP_000369.3:p.Ser262ThrfsTer25
NM_000378.5:c.796_797dup	NP_000369.4:p.Ser267ThrfsTer25
NM_000378.6:c.796_797dup	NP_000369.4:p.Ser267ThrfsTer25
NM_001198551.1:c.145_146dup , LRG_525t2:c.145_146dup	NP_001185480.1:p.Ser50ThrfsTer25
NM_001198552.1:c.145_146dup	NP_001185481.1:p.Ser50ThrfsTer25
NM_001198552.2:c.145_146dup	NP_001185481.1:p.Ser50ThrfsTer25
NM_024424.3:c.781_782dup	NP_077742.2:p.Ser262ThrfsTer25
NM_024424.4:c.796_797dup	NP_077742.3:p.Ser267ThrfsTer25
NM_024424.5:c.796_797dup	NP_077742.3:p.Ser267ThrfsTer25
NM_024426.4:c.781_782dup	NP_077744.3:p.Ser262ThrfsTer25
NM_024426.5:c.796_797dup	NP_077744.4:p.Ser267ThrfsTer25
NR_160306.1:n.975_976dup
ENST00000332351.7:c.781_782dup	ENSP00000331327.3:p.Ser262ThrfsTer25
ENST00000332351.9:c.796_797dup	ENSP00000331327.5:p.Ser267ThrfsTer25
ENST00000379077.7:c.781_782dup	ENSP00000368368.3:p.Ser262ThrfsTer25
ENST00000379077.9:c.796_797dup	ENSP00000368368.5:p.Ser267ThrfsTer25
ENST00000379079.6:c.145_146dup	ENSP00000368370.2:p.Ser50ThrfsTer25
ENST00000379079.8:c.145_146dup	ENSP00000368370.2:p.Ser50ThrfsTer25
ENST00000448076.7:c.781_782dup	ENSP00000413452.3:p.Ser262ThrfsTer25
ENST00000448076.9:c.796_797dup	ENSP00000413452.5:p.Ser267ThrfsTer25
ENST00000452863.7:c.781_782dup	ENSP00000415516.3:p.Ser262ThrfsTer25
ENST00000527775.1:c.34_35dup	ENSP00000435351.1:p.Ser13ThrfsTer25
ENST00000530998.5:c.145_146dup	ENSP00000435307.1:p.Ser50ThrfsTer25
ENST00000639563.3:c.796_797dup	ENSP00000492269.3:p.Ser267ThrfsTer25
ENST00000640146.2:c.172_173dup	ENSP00000491984.2:p.Ser59ThrfsTer25