Canonical Allele Identifier: CA219496227

Gene: WT1

Linked Data

• ClinVar Variation Id: 1019245
• ClinVar RCV Id: RCV001318661
• dbSNP Id: rs907964605
• MyVariant Identifiers: chr11:g.32439195T>C (hg19) ; chr11:g.32417649T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417649T>C , CM000673.2:g.32417649T>C	GRCh38
NC_000011.9:g.32439195T>C , CM000673.1:g.32439195T>C	GRCh37
NC_000011.8:g.32395771T>C	NCBI36
NG_009272.1:g.22893A>G , LRG_525:g.22893A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.893A>G	ENSP00000331327.5:p.Asn298Ser
ENST00000379077.9:c.893A>G	ENSP00000368368.5:p.Asn298Ser
ENST00000379079.8:c.242A>G	ENSP00000368370.2:p.Asn81Ser
ENST00000448076.9:c.893A>G	ENSP00000413452.5:p.Asn298Ser
ENST00000452863.10:c.893A>G MANE Select	ENSP00000415516.5:p.Asn298Ser
ENST00000639563.3:c.893A>G	ENSP00000492269.3:p.Asn298Ser
ENST00000640146.2:c.269A>G	ENSP00000491984.2:p.Asn90Ser
ENST00000332351.7:c.878A>G	ENSP00000331327.3:p.Asn293Ser
ENST00000379077.7:c.878A>G	ENSP00000368368.3:p.Asn293Ser
ENST00000379079.6:c.242A>G	ENSP00000368370.2:p.Asn81Ser
ENST00000448076.7:c.878A>G	ENSP00000413452.3:p.Asn293Ser
ENST00000452863.7:c.878A>G	ENSP00000415516.3:p.Asn293Ser
ENST00000527775.1:c.131A>G	ENSP00000435351.1:p.Asn44Ser
ENST00000530998.5:c.242A>G	ENSP00000435307.1:p.Asn81Ser
NM_000378.4:c.878A>G	NP_000369.3:p.Asn293Ser
NM_001198551.1:c.242A>G , LRG_525t2:c.242A>G	NP_001185480.1:p.Asn81Ser
NM_001198552.1:c.242A>G	NP_001185481.1:p.Asn81Ser
NM_024424.3:c.878A>G	NP_077742.2:p.Asn293Ser
NM_024426.4:c.878A>G	NP_077744.3:p.Asn293Ser
NM_000378.5:c.893A>G	NP_000369.4:p.Asn298Ser
NM_024424.4:c.893A>G	NP_077742.3:p.Asn298Ser
NM_024426.5:c.893A>G	NP_077744.4:p.Asn298Ser
NR_160306.1:n.1072A>G
NM_000378.6:c.893A>G	NP_000369.4:p.Asn298Ser
NM_001198552.2:c.242A>G	NP_001185481.1:p.Asn81Ser
NM_024424.5:c.893A>G	NP_077742.3:p.Asn298Ser
NM_024426.6:c.893A>G MANE Select	NP_077744.4:p.Asn298Ser