Canonical Allele Identifier: CA379961976

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417575A>G , CM000673.2:g.32417575A>G	GRCh38
NC_000011.9:g.32439121A>G , CM000673.1:g.32439121A>G	GRCh37
NC_000011.8:g.32395697A>G	NCBI36
NG_009272.1:g.22967T>C , LRG_525:g.22967T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.965+2T>C MANE Select	NP_077744.4:n.965+2T>C
ENST00000452863.10:c.965+2T>C MANE Select	ENSP00000415516.5:n.965+2T>C
NM_000378.4:c.950+2T>C	NP_000369.3:n.950+2T>C
NM_000378.5:c.965+2T>C	NP_000369.4:n.965+2T>C
NM_000378.6:c.965+2T>C	NP_000369.4:n.965+2T>C
NM_001198551.1:c.314+2T>C , LRG_525t2:c.314+2T>C	NP_001185480.1:n.314+2T>C
NM_001198552.1:c.314+2T>C	NP_001185481.1:n.314+2T>C
NM_001198552.2:c.314+2T>C	NP_001185481.1:n.314+2T>C
NM_024424.3:c.950+2T>C	NP_077742.2:n.950+2T>C
NM_024424.4:c.965+2T>C	NP_077742.3:n.965+2T>C
NM_024424.5:c.965+2T>C	NP_077742.3:n.965+2T>C
NM_024426.4:c.950+2T>C	NP_077744.3:n.950+2T>C
NM_024426.5:c.965+2T>C	NP_077744.4:n.965+2T>C
NR_160306.1:n.1146T>C
ENST00000332351.7:c.950+2T>C	ENSP00000331327.3:n.950+2T>C
ENST00000332351.9:c.965+2T>C	ENSP00000331327.5:n.965+2T>C
ENST00000379077.7:c.952T>C	ENSP00000368368.3:p.Ter318Gln
ENST00000379077.9:c.967T>C	ENSP00000368368.5:p.Ter323Gln
ENST00000379079.6:c.314+2T>C	ENSP00000368370.2:n.314+2T>C
ENST00000379079.8:c.314+2T>C	ENSP00000368370.2:n.314+2T>C
ENST00000448076.7:c.950+2T>C	ENSP00000413452.3:n.950+2T>C
ENST00000448076.9:c.965+2T>C	ENSP00000413452.5:n.965+2T>C
ENST00000452863.7:c.950+2T>C	ENSP00000415516.3:n.950+2T>C
ENST00000527775.1:c.203+2T>C	ENSP00000435351.1:n.203+2T>C
ENST00000527882.5:c.21+2T>C
ENST00000530998.5:c.314+2T>C	ENSP00000435307.1:n.314+2T>C
ENST00000639563.3:c.965+2T>C	ENSP00000492269.3:n.965+2T>C
ENST00000640146.2:c.341+2T>C	ENSP00000491984.2:n.341+2T>C