Canonical Allele Identifier: CA1962318461
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32417642G= , CM000673.2:g.32417642G= GRCh38
NC_000011.9:g.32439188G= , CM000673.1:g.32439188G= GRCh37
NC_000011.8:g.32395764G= NCBI36
NG_009272.1:g.22900C= , LRG_525:g.22900C=

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.900C= ENSP00000331327.5:p.Tyr300=
ENST00000379077.9:c.900C= ENSP00000368368.5:p.Tyr300=
ENST00000379079.8:c.249C= ENSP00000368370.2:p.Tyr83=
ENST00000448076.9:c.900C= ENSP00000413452.5:p.Tyr300=
ENST00000452863.10:c.900C= MANE Select ENSP00000415516.5:p.Tyr300=
ENST00000639563.3:c.900C= ENSP00000492269.3:p.Tyr300=
ENST00000640146.2:c.276C= ENSP00000491984.2:p.Tyr92=
ENST00000332351.7:c.885C= ENSP00000331327.3:p.Tyr295=
ENST00000379077.7:c.885C= ENSP00000368368.3:p.Tyr295=
ENST00000379079.6:c.249C= ENSP00000368370.2:p.Tyr83=
ENST00000448076.7:c.885C= ENSP00000413452.3:p.Tyr295=
ENST00000452863.7:c.885C= ENSP00000415516.3:p.Tyr295=
ENST00000527775.1:c.138C= ENSP00000435351.1:p.Tyr46=
ENST00000530998.5:c.249C= ENSP00000435307.1:p.Tyr83=
NM_000378.4:c.885C= NP_000369.3:p.Tyr295=
NM_001198551.1:c.249C= , LRG_525t2:c.249C= NP_001185480.1:p.Tyr83=
NM_001198552.1:c.249C= NP_001185481.1:p.Tyr83=
NM_024424.3:c.885C= NP_077742.2:p.Tyr295=
NM_024426.4:c.885C= NP_077744.3:p.Tyr295=
NM_000378.5:c.900C= NP_000369.4:p.Tyr300=
NM_024424.4:c.900C= NP_077742.3:p.Tyr300=
NM_024426.5:c.900C= NP_077744.4:p.Tyr300=
NR_160306.1:n.1079C=
NM_000378.6:c.900C= NP_000369.4:p.Tyr300=
NM_001198552.2:c.249C= NP_001185481.1:p.Tyr83=
NM_024424.5:c.900C= NP_077742.3:p.Tyr300=
NM_024426.6:c.900C= MANE Select NP_077744.4:p.Tyr300=