Canonical Allele Identifier: CA065442

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428607A>G , CM000673.2:g.32428607A>G	GRCh38
NC_000011.9:g.32450153A>G , CM000673.1:g.32450153A>G	GRCh37
NC_000011.8:g.32406729A>G	NCBI36
NG_009272.1:g.11935T>C , LRG_525:g.11935T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.674T>C MANE Select	NP_077744.4:p.Val225Ala
ENST00000452863.10:c.674T>C MANE Select	ENSP00000415516.5:p.Val225Ala
NM_000378.4:c.659T>C	NP_000369.3:p.Val220Ala
NM_000378.5:c.674T>C	NP_000369.4:p.Val225Ala
NM_000378.6:c.674T>C	NP_000369.4:p.Val225Ala
NM_001198551.1:c.23T>C , LRG_525t2:c.23T>C	NP_001185480.1:p.Val8Ala
NM_001198552.1:c.23T>C	NP_001185481.1:p.Val8Ala
NM_001198552.2:c.23T>C	NP_001185481.1:p.Val8Ala
NM_024424.3:c.659T>C	NP_077742.2:p.Val220Ala
NM_024424.4:c.674T>C	NP_077742.3:p.Val225Ala
NM_024424.5:c.674T>C	NP_077742.3:p.Val225Ala
NM_024426.4:c.659T>C	NP_077744.3:p.Val220Ala
NM_024426.5:c.674T>C	NP_077744.4:p.Val225Ala
NR_160306.1:n.853T>C
ENST00000332351.7:c.659T>C	ENSP00000331327.3:p.Val220Ala
ENST00000332351.9:c.674T>C	ENSP00000331327.5:p.Val225Ala
ENST00000379077.7:c.659T>C	ENSP00000368368.3:p.Val220Ala
ENST00000379077.9:c.674T>C	ENSP00000368368.5:p.Val225Ala
ENST00000379079.6:c.23T>C	ENSP00000368370.2:p.Val8Ala
ENST00000379079.8:c.23T>C	ENSP00000368370.2:p.Val8Ala
ENST00000448076.7:c.659T>C	ENSP00000413452.3:p.Val220Ala
ENST00000448076.9:c.674T>C	ENSP00000413452.5:p.Val225Ala
ENST00000452863.7:c.659T>C	ENSP00000415516.3:p.Val220Ala
ENST00000527775.1:c.-89T>C	ENSP00000435351.1:n.-89T>C
ENST00000530998.5:c.23T>C	ENSP00000435307.1:p.Val8Ala
ENST00000639563.3:c.674T>C	ENSP00000492269.3:p.Val225Ala
ENST00000640146.2:c.50T>C	ENSP00000491984.2:p.Val17Ala