Canonical Allele Identifier: CA13440148

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32430375G>C , CM000673.2:g.32430375G>C	GRCh38
NC_000011.9:g.32451921G>C , CM000673.1:g.32451921G>C	GRCh37
NC_000011.8:g.32408497G>C	NCBI36
NG_009272.1:g.10167C>G , LRG_525:g.10167C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.662-1756C>G	ENSP00000331327.5:n.662-1756C>G
ENST00000379077.9:c.662-1756C>G	ENSP00000368368.5:n.662-1756C>G
ENST00000379079.8:c.10+155C>G	ENSP00000368370.2:n.10+155C>G
ENST00000448076.9:c.662-1756C>G	ENSP00000413452.5:n.662-1756C>G
ENST00000452863.10:c.662-1756C>G MANE Select	ENSP00000415516.5:n.662-1756C>G
ENST00000639563.3:c.662-1756C>G	ENSP00000492269.3:n.662-1756C>G
ENST00000640146.2:c.38-1756C>G	ENSP00000491984.2:n.38-1756C>G
ENST00000332351.7:c.647-1756C>G	ENSP00000331327.3:n.647-1756C>G
ENST00000379077.7:c.647-1756C>G	ENSP00000368368.3:n.647-1756C>G
ENST00000379079.6:c.10+155C>G	ENSP00000368370.2:n.10+155C>G
ENST00000448076.7:c.647-1756C>G	ENSP00000413452.3:n.647-1756C>G
ENST00000452863.7:c.647-1756C>G	ENSP00000415516.3:n.647-1756C>G
ENST00000530998.5:c.10+155C>G	ENSP00000435307.1:n.10+155C>G
NM_000378.4:c.647-1756C>G	NP_000369.3:n.647-1756C>G
NM_001198551.1:c.10+155C>G , LRG_525t2:c.10+155C>G	NP_001185480.1:n.10+155C>G
NM_001198552.1:c.10+155C>G	NP_001185481.1:n.10+155C>G
NM_024424.3:c.647-1756C>G	NP_077742.2:n.647-1756C>G
NM_024426.4:c.647-1756C>G	NP_077744.3:n.647-1756C>G
NM_000378.5:c.662-1756C>G	NP_000369.4:n.662-1756C>G
NM_024424.4:c.662-1756C>G	NP_077742.3:n.662-1756C>G
NM_024426.5:c.662-1756C>G	NP_077744.4:n.662-1756C>G
NR_160306.1:n.841-1756C>G
NM_000378.6:c.662-1756C>G	NP_000369.4:n.662-1756C>G
NM_001198552.2:c.10+155C>G	NP_001185481.1:n.10+155C>G
NM_024424.5:c.662-1756C>G	NP_077742.3:n.662-1756C>G
NM_024426.6:c.662-1756C>G MANE Select	NP_077744.4:n.662-1756C>G