Canonical Allele Identifier: CA1962317966
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32387951T= , CM000673.2:g.32387951T= GRCh38
NC_000011.9:g.32409497T= , CM000673.1:g.32409497T= GRCh37
NC_000011.8:g.32366073T= NCBI36
NG_009272.1:g.52591A= , LRG_525:g.52591A=

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.*1107A= ENSP00000331327.5:n.*1107A=
ENST00000379077.9:c.*1860A= ENSP00000368368.5:n.*1860A=
ENST00000379079.8:c.*1107A= ENSP00000368370.2:n.*1107A=
ENST00000452863.10:c.*1107A= MANE Select ENSP00000415516.5:n.*1107A=
ENST00000651819.1:n.1601A=
ENST00000332351.7:c.*1107A= ENSP00000331327.3:n.*1107A=
ENST00000379077.7:c.*1860A= ENSP00000368368.3:n.*1860A=
ENST00000379079.6:c.*1107A= ENSP00000368370.2:n.*1107A=
ENST00000452863.7:c.2601A= ENSP00000415516.3:n.2601A=
ENST00000530998.5:c.*1107A= ENSP00000435307.1:n.*1107A=
NM_000378.4:c.*1107A= NP_000369.3:n.*1107A=
NM_001198551.1:c.*1107A= , LRG_525t2:c.*1107A= NP_001185480.1:n.*1107A=
NM_001198552.1:c.*1107A= NP_001185481.1:n.*1107A=
NM_024424.3:c.*1107A= NP_077742.2:n.*1107A=
NM_024426.4:c.*1107A= NP_077744.3:n.*1107A=
NM_000378.5:c.*1107A= NP_000369.4:n.*1107A=
NM_024424.4:c.*1107A= NP_077742.3:n.*1107A=
NM_024426.5:c.*1107A= NP_077744.4:n.*1107A=
NM_001367854.1:c.*1107A= NP_001354783.1:n.*1107A=
NR_160306.1:n.3008A=
NM_000378.6:c.*1107A= NP_000369.4:n.*1107A=
NM_001198552.2:c.*1107A= NP_001185481.1:n.*1107A=
NM_024424.5:c.*1107A= NP_077742.3:n.*1107A=
NM_024426.6:c.*1107A= MANE Select NP_077744.4:n.*1107A=