Canonical Allele Identifier: CA1962318522
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32417807T= , CM000673.2:g.32417807T= GRCh38
NC_000011.9:g.32439353T= , CM000673.1:g.32439353T= GRCh37
NC_000011.8:g.32395929T= NCBI36
NG_009272.1:g.22735A= , LRG_525:g.22735A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.888-153A= ENSP00000331327.5:n.888-153A=
ENST00000379077.9:c.888-153A= ENSP00000368368.5:n.888-153A=
ENST00000379079.8:c.237-153A= ENSP00000368370.2:n.237-153A=
ENST00000448076.9:c.888-153A= ENSP00000413452.5:n.888-153A=
ENST00000452863.10:c.888-153A= MANE Select ENSP00000415516.5:n.888-153A=
ENST00000639563.3:c.888-153A= ENSP00000492269.3:n.888-153A=
ENST00000640146.2:c.264-153A= ENSP00000491984.2:n.264-153A=
ENST00000332351.7:c.873-153A= ENSP00000331327.3:n.873-153A=
ENST00000379077.7:c.873-153A= ENSP00000368368.3:n.873-153A=
ENST00000379079.6:c.237-153A= ENSP00000368370.2:n.237-153A=
ENST00000448076.7:c.873-153A= ENSP00000413452.3:n.873-153A=
ENST00000452863.7:c.873-153A= ENSP00000415516.3:n.873-153A=
ENST00000527775.1:c.126-153A= ENSP00000435351.1:n.126-153A=
ENST00000530998.5:c.237-153A= ENSP00000435307.1:n.237-153A=
NM_000378.4:c.873-153A= NP_000369.3:n.873-153A=
NM_001198551.1:c.237-153A= , LRG_525t2:c.237-153A= NP_001185480.1:n.237-153A=
NM_001198552.1:c.237-153A= NP_001185481.1:n.237-153A=
NM_024424.3:c.873-153A= NP_077742.2:n.873-153A=
NM_024426.4:c.873-153A= NP_077744.3:n.873-153A=
NM_000378.5:c.888-153A= NP_000369.4:n.888-153A=
NM_024424.4:c.888-153A= NP_077742.3:n.888-153A=
NM_024426.5:c.888-153A= NP_077744.4:n.888-153A=
NR_160306.1:n.1067-153A=
NM_000378.6:c.888-153A= NP_000369.4:n.888-153A=
NM_001198552.2:c.237-153A= NP_001185481.1:n.237-153A=
NM_024424.5:c.888-153A= NP_077742.3:n.888-153A=
NM_024426.6:c.888-153A= MANE Select NP_077744.4:n.888-153A=