Canonical Allele Identifier: CA379962210

Gene: WT1

Linked Data

• COSMIC: COSM4032375 ; COSM4032376 ; COSM4907101
• MyVariant Identifiers: chr11:g.32439194A>C (hg19) ; chr11:g.32417648A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417648A>C , CM000673.2:g.32417648A>C	GRCh38
NC_000011.9:g.32439194A>C , CM000673.1:g.32439194A>C	GRCh37
NC_000011.8:g.32395770A>C	NCBI36
NG_009272.1:g.22894T>G , LRG_525:g.22894T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.894T>G	ENSP00000331327.5:p.Asn298Lys
ENST00000379077.9:c.894T>G	ENSP00000368368.5:p.Asn298Lys
ENST00000379079.8:c.243T>G	ENSP00000368370.2:p.Asn81Lys
ENST00000448076.9:c.894T>G	ENSP00000413452.5:p.Asn298Lys
ENST00000452863.10:c.894T>G MANE Select	ENSP00000415516.5:p.Asn298Lys
ENST00000639563.3:c.894T>G	ENSP00000492269.3:p.Asn298Lys
ENST00000640146.2:c.270T>G	ENSP00000491984.2:p.Asn90Lys
ENST00000332351.7:c.879T>G	ENSP00000331327.3:p.Asn293Lys
ENST00000379077.7:c.879T>G	ENSP00000368368.3:p.Asn293Lys
ENST00000379079.6:c.243T>G	ENSP00000368370.2:p.Asn81Lys
ENST00000448076.7:c.879T>G	ENSP00000413452.3:p.Asn293Lys
ENST00000452863.7:c.879T>G	ENSP00000415516.3:p.Asn293Lys
ENST00000527775.1:c.132T>G	ENSP00000435351.1:p.Asn44Lys
ENST00000530998.5:c.243T>G	ENSP00000435307.1:p.Asn81Lys
NM_000378.4:c.879T>G	NP_000369.3:p.Asn293Lys
NM_001198551.1:c.243T>G , LRG_525t2:c.243T>G	NP_001185480.1:p.Asn81Lys
NM_001198552.1:c.243T>G	NP_001185481.1:p.Asn81Lys
NM_024424.3:c.879T>G	NP_077742.2:p.Asn293Lys
NM_024426.4:c.879T>G	NP_077744.3:p.Asn293Lys
NM_000378.5:c.894T>G	NP_000369.4:p.Asn298Lys
NM_024424.4:c.894T>G	NP_077742.3:p.Asn298Lys
NM_024426.5:c.894T>G	NP_077744.4:p.Asn298Lys
NR_160306.1:n.1073T>G
NM_000378.6:c.894T>G	NP_000369.4:p.Asn298Lys
NM_001198552.2:c.243T>G	NP_001185481.1:p.Asn81Lys
NM_024424.5:c.894T>G	NP_077742.3:p.Asn298Lys
NM_024426.6:c.894T>G MANE Select	NP_077744.4:p.Asn298Lys