Canonical Allele Identifier: CA1962327490

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435366C= , CM000673.2:g.32435366C=	GRCh38
NC_000011.9:g.32456912C= , CM000673.1:g.32456912C=	GRCh37
NC_000011.8:g.32413488C=	NCBI36
NG_009272.1:g.5176G= , LRG_525:g.5176G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.-6G=	ENSP00000331327.5:n.-6G=
ENST00000379077.9:c.-6G=	ENSP00000368368.5:n.-6G=
ENST00000448076.9:c.-6G=	ENSP00000413452.5:n.-6G=
ENST00000452863.10:c.-6G= MANE Select	ENSP00000415516.5:n.-6G=
ENST00000332351.7:c.-21G=	ENSP00000331327.3:n.-21G=
ENST00000379077.7:c.-21G=	ENSP00000368368.3:n.-21G=
ENST00000448076.7:c.-21G=	ENSP00000413452.3:n.-21G=
NM_000378.4:c.-21G=	NP_000369.3:n.-21G=
NM_024424.3:c.-21G=	NP_077742.2:n.-21G=
NM_024426.4:c.-21G=	NP_077744.3:n.-21G=
NM_000378.5:c.-6G=	NP_000369.4:n.-6G=
NM_024424.4:c.-6G=	NP_077742.3:n.-6G=
NM_024426.5:c.-6G=	NP_077744.4:n.-6G=
NR_160306.1:n.174G=
NM_000378.6:c.-6G=	NP_000369.4:n.-6G=
NM_024424.5:c.-6G=	NP_077742.3:n.-6G=
NM_024426.6:c.-6G= MANE Select	NP_077744.4:n.-6G=