Canonical Allele Identifier: CA1962327424

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435249C= , CM000673.2:g.32435249C=	GRCh38
NC_000011.9:g.32456795C= , CM000673.1:g.32456795C=	GRCh37
NC_000011.8:g.32413371C=	NCBI36
NG_009272.1:g.5293G= , LRG_525:g.5293G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.112G=	ENSP00000331327.5:p.Val38=
ENST00000379077.9:c.112G=	ENSP00000368368.5:p.Val38=
ENST00000448076.9:c.112G=	ENSP00000413452.5:p.Val38=
ENST00000452863.10:c.112G= MANE Select	ENSP00000415516.5:p.Val38=
ENST00000639563.3:c.112G=	ENSP00000492269.3:p.Val38=
ENST00000332351.7:c.97G=	ENSP00000331327.3:p.Val33=
ENST00000379077.7:c.97G=	ENSP00000368368.3:p.Val33=
ENST00000448076.7:c.97G=	ENSP00000413452.3:p.Val33=
ENST00000452863.7:c.97G=	ENSP00000415516.3:p.Val33=
NM_000378.4:c.97G=	NP_000369.3:p.Val33=
NM_024424.3:c.97G=	NP_077742.2:p.Val33=
NM_024426.4:c.97G=	NP_077744.3:p.Val33=
NM_000378.5:c.112G=	NP_000369.4:p.Val38=
NM_024424.4:c.112G=	NP_077742.3:p.Val38=
NM_024426.5:c.112G=	NP_077744.4:p.Val38=
NR_160306.1:n.291G=
NM_000378.6:c.112G=	NP_000369.4:p.Val38=
NM_024424.5:c.112G=	NP_077742.3:p.Val38=
NM_024426.6:c.112G= MANE Select	NP_077744.4:p.Val38=