Canonical Allele Identifier: CA379958866

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392024G>T , CM000673.2:g.32392024G>T	GRCh38
NC_000011.9:g.32413570G>T , CM000673.1:g.32413570G>T	GRCh37
NC_000011.8:g.32370146G>T	NCBI36
NG_009272.1:g.48518C>A , LRG_525:g.48518C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1344C>A	ENSP00000331327.5:p.Phe448Leu
ENST00000379077.9:c.*579C>A	ENSP00000368368.5:n.*579C>A
ENST00000379079.8:c.744C>A	ENSP00000368370.2:p.Phe248Leu
ENST00000448076.9:c.1395C>A	ENSP00000413452.5:p.Phe465Leu
ENST00000452863.10:c.1395C>A MANE Select	ENSP00000415516.5:p.Phe465Leu
ENST00000526685.2:n.849C>A
ENST00000639563.3:c.1344C>A	ENSP00000492269.3:p.Phe448Leu
ENST00000639907.2:n.538C>A
ENST00000640146.2:c.720C>A	ENSP00000491984.2:p.Phe240Leu
ENST00000650745.1:n.1205C>A
ENST00000650861.1:n.1976C>A
ENST00000650986.1:n.58C>A
ENST00000651459.1:c.166C>A
ENST00000651533.1:n.441C>A
ENST00000651668.1:n.332C>A
ENST00000651794.1:n.1238C>A
ENST00000651819.1:n.320C>A
ENST00000652579.1:n.655C>A
ENST00000652724.1:n.585C>A
ENST00000332351.7:c.1380C>A	ENSP00000331327.3:p.Phe460Leu
ENST00000379077.7:c.*579C>A	ENSP00000368368.3:n.*579C>A
ENST00000379079.6:c.744C>A	ENSP00000368370.2:p.Phe248Leu
ENST00000448076.7:c.1380C>A	ENSP00000413452.3:p.Phe460Leu
ENST00000452863.7:c.1329C>A	ENSP00000415516.3:p.Phe443Leu
ENST00000527882.5:c.361C>A
ENST00000530998.5:c.693C>A	ENSP00000435307.1:p.Phe231Leu
NM_000378.4:c.1329C>A	NP_000369.3:p.Phe443Leu
NM_001198551.1:c.744C>A , LRG_525t2:c.744C>A	NP_001185480.1:p.Phe248Leu
NM_001198552.1:c.693C>A	NP_001185481.1:p.Phe231Leu
NM_024424.3:c.1380C>A	NP_077742.2:p.Phe460Leu
NM_024426.4:c.1380C>A	NP_077744.3:p.Phe460Leu
NM_000378.5:c.1344C>A	NP_000369.4:p.Phe448Leu
NM_024424.4:c.1395C>A	NP_077742.3:p.Phe465Leu
NM_024426.5:c.1395C>A	NP_077744.4:p.Phe465Leu
NM_001367854.1:c.207C>A	NP_001354783.1:p.Phe69Leu
NR_160306.1:n.1727C>A
NM_000378.6:c.1344C>A	NP_000369.4:p.Phe448Leu
NM_001198552.2:c.693C>A	NP_001185481.1:p.Phe231Leu
NM_024424.5:c.1395C>A	NP_077742.3:p.Phe465Leu
NM_024426.6:c.1395C>A MANE Select	NP_077744.4:p.Phe465Leu