Canonical Allele Identifier: CA065682

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428011G>C , CM000673.2:g.32428011G>C	GRCh38
NC_000011.9:g.32449557G>C , CM000673.1:g.32449557G>C	GRCh37
NC_000011.8:g.32406133G>C	NCBI36
NG_009272.1:g.12531C>G , LRG_525:g.12531C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.832C>G MANE Select	NP_077744.4:p.Pro278Ala
ENST00000452863.10:c.832C>G MANE Select	ENSP00000415516.5:p.Pro278Ala
NM_000378.4:c.817C>G	NP_000369.3:p.Pro273Ala
NM_000378.5:c.832C>G	NP_000369.4:p.Pro278Ala
NM_000378.6:c.832C>G	NP_000369.4:p.Pro278Ala
NM_001198551.1:c.181C>G , LRG_525t2:c.181C>G	NP_001185480.1:p.Pro61Ala
NM_001198552.1:c.181C>G	NP_001185481.1:p.Pro61Ala
NM_001198552.2:c.181C>G	NP_001185481.1:p.Pro61Ala
NM_024424.3:c.817C>G	NP_077742.2:p.Pro273Ala
NM_024424.4:c.832C>G	NP_077742.3:p.Pro278Ala
NM_024424.5:c.832C>G	NP_077742.3:p.Pro278Ala
NM_024426.4:c.817C>G	NP_077744.3:p.Pro273Ala
NM_024426.5:c.832C>G	NP_077744.4:p.Pro278Ala
NR_160306.1:n.1011C>G
ENST00000332351.7:c.817C>G	ENSP00000331327.3:p.Pro273Ala
ENST00000332351.9:c.832C>G	ENSP00000331327.5:p.Pro278Ala
ENST00000379077.7:c.817C>G	ENSP00000368368.3:p.Pro273Ala
ENST00000379077.9:c.832C>G	ENSP00000368368.5:p.Pro278Ala
ENST00000379079.6:c.181C>G	ENSP00000368370.2:p.Pro61Ala
ENST00000379079.8:c.181C>G	ENSP00000368370.2:p.Pro61Ala
ENST00000448076.7:c.817C>G	ENSP00000413452.3:p.Pro273Ala
ENST00000448076.9:c.832C>G	ENSP00000413452.5:p.Pro278Ala
ENST00000452863.7:c.817C>G	ENSP00000415516.3:p.Pro273Ala
ENST00000527775.1:c.70C>G	ENSP00000435351.1:p.Pro24Ala
ENST00000530998.5:c.181C>G	ENSP00000435307.1:p.Pro61Ala
ENST00000639563.3:c.832C>G	ENSP00000492269.3:p.Pro278Ala
ENST00000640146.2:c.208C>G	ENSP00000491984.2:p.Pro70Ala